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Herman Van Den Berghe

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Co-Publications
Name
96
Dal Cin, Paola
83
Cassiman, Jean-Jacques
68
Mecucci, Cristina
45
Wlodarska, Iwona
44
Sciot, Raf
41
Marynen, Peter
32
De Wever, Ivo
29
Stul, Michel
29
Van Leuven, Fred
28
De Wolf-Peeters, Christiane
25
Louwagie, Andries
24
Michaux, JL
23
Verhoef, Gregor
22
Dierlamm, Judith
21
Boogaerts, Marc

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Publications

TOP 3
Mertens Fredrik; Strömberg Ulf; Mandahl Nils; Dal Cin Paola; De Wever Ivo; Fletcher Christopher D M; Mitelman Felix; Rosai Juan; Rydholm Anders; Sciot Raf; Tallini Giovanni; Van Den Berghe Herman; Vanni Roberta; Willén Helena
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group.
Tallini Giovanni; Dorfman Howard; Brys Peter; Dal Cin Paola; De Wever Ivo; Fletcher Christopher D M; Jonson Kjell; Mandahl Nils; Mertens Fredrik; Mitelman Felix; Rosai Juan; Rydholm Anders; Samson Ignace; Sciot Raf; Van den Berghe Herman; Vanni Roberta; Willén Helena
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
Koontz J I; Soreng A L; Nucci M; Kuo F C; Pauwels P; van Den Berghe H; Dal Cin P; Fletcher J A; Sklar J
Frequent fusion of the JAZF1 and JJAZ1 genes in endometrial stromal tumors.

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All Publications

2002: Mertens Fredrik; Strömberg Ulf; Mandahl Nils; Dal Cin Paola; De Wever Ivo; Fletcher Christopher D M; Mitelman Felix; Rosai Juan; Rydholm Anders; Sciot Raf; Tallini Giovanni; Van Den Berghe Herman; Vanni Roberta; Willén Helena
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group.
Cancer research 2002;62(14):3980-4.
2002: Tallini Giovanni; Dorfman Howard; Brys Peter; Dal Cin Paola; De Wever Ivo; Fletcher Christopher D M; Jonson Kjell; Mandahl Nils; Mertens Fredrik; Mitelman Felix; Rosai Juan; Rydholm Anders; Samson Ignace; Sciot Raf; Van den Berghe Herman; Vanni Roberta; Willén Helena
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
The Journal of pathology 2002;196(2):194-203.
2001: Koontz J I; Soreng A L; Nucci M; Kuo F C; Pauwels P; van Den Berghe H; Dal Cin P; Fletcher J A; Sklar J
Frequent fusion of the JAZF1 and JJAZ1 genes in endometrial stromal tumors.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(11):6348-53.
2000: Sciot R; Dorfman H; Brys P; Dal Cin P; De Wever I; Fletcher C D; Jonson K; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Samson I; Tallini G; Van den Berghe H; Vanni R; Willén H
Cytogenetic-morphologic correlations in aneurysmal bone cyst, giant cell tumor of bone and combined lesions. A report from the CHAMP study group.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2000;13(11):1206-10.
2000: Dal Cin P; Sciot R; Brys P; De Wever I; Dorfman H; Fletcher C D; Jonsson K; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Samson I; Tallini G; Van den Berghe H; Vanni R; Willen H
Recurrent chromosome aberrations in fibrous dysplasia of the bone: a report of the CHAMP study group. CHromosomes And MorPhology.
Cancer genetics and cytogenetics 2000;122(1):30-2.
2000: De Wever I; Dal Cin P; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van Den Berghe H; Vanni R; Willén H
Cytogenetic, clinical, and morphologic correlations in 78 cases of fibromatosis: a report from the CHAMP Study Group. CHromosomes And Morphology.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2000;13(10):1080-5.
2000: Dierlamm J; Stefanova M; Wlodarska I; Hinz K; Maes B; Michaux L; Stul M; Verhoef G; Thomas J; De Wolf-Peeters C; Van den Berghe H; Hossfeld D K; Hagemeijer A
Analysis of the P53, RB/D13S25, and P16 tumor suppressor genes in marginal zone B-cell lymphoma: An interphase fluorescence in situ hybridization study.
Cancer genetics and cytogenetics 2000;120(1):1-5.
2000: Dierlamm J; Wlodarska I; Michaux L; Stefanova M; Hinz K; Van Den Berghe H; Hagemeijer A; Hossfeld D K
Genetic abnormalities in marginal zone B-cell lymphoma.
Hematological oncology 2000;18(1):1-13.
2000: Tallini G; Vanni R; Manfioletti G; Kazmierczak B; Faa G; Pauwels P; Bullerdiek J; Giancotti V; Van Den Berghe H; Dal Cin P
HMGI-C and HMGI(Y) immunoreactivity correlates with cytogenetic abnormalities in lipomas, pulmonary chondroid hamartomas, endometrial polyps, and uterine leiomyomas and is compatible with rearrangement of the HMGI-C and HMGI(Y) genes.
Laboratory investigation; a journal of technical methods and pathology 2000;80(3):359-69.
2000: Mertens F; Dal Cin P; De Wever I; Fletcher C D; Mandahl N; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; van Den Berghe H; Vanni R; Willén H
Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group.
The Journal of pathology 2000;190(1):31-8.
2000: Kazmierczak B; Dal Cin P; Rogalla P; Van den Berghe H; Bullerdiek J
Regional fine mapping of HMG17 to chromosomal band 1p35.
Cancer genetics and cytogenetics 2000;116(2):164-5.
2000: Mandahl N; Fletcher C D; Dal Cin P; De Wever I; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van Den Berghe H; Vanni R; Willén H
Comparative cytogenetic study of spindle cell and pleomorphic leiomyosarcomas of soft tissues: a report from the CHAMP Study Group.
Cancer genetics and cytogenetics 2000;116(1):66-73.
2000: Dal Cin P; Roskams T; De Vos R; Van Poppel H; Balzarini P; Van Den Berghe H
Involvement of chromosomes 1 and 18 in renal cell tumors.
Cancer genetics and cytogenetics 2000;116(1):54-8.
1999: Dal Cin P; Roskams T; Van Poppel H; Balzarini P; Van den Berghe H
Cytogenetic investigation of transitional cell carcinomas of the upper urinary tract.
Cancer genetics and cytogenetics 1999;114(2):117-20.
1999: Kazmierczak B; Dal Cin P; Sciot R; Van den Berghe H; Bullerdiek J
Inflammatory myofibroblastic tumor with HMGIC rearrangement.
Cancer genetics and cytogenetics 1999;112(2):156-60.
1999: Van den Berghe I; Dal Cin P; De Groef K; Michielssen P; Van den Berghe H
Monosomy 22 and trisomy 14 may be early events in the tumorigenesis of adult granulosa cell tumor.
Cancer genetics and cytogenetics 1999;112(1):46-8.
1999: Sciot R; Dal Cin P; Hagemeijer A; De Smet L; Van Damme B; Van den Berghe H
Cutaneous sclerosing perineurioma with cryptic NF2 gene deletion.
The American journal of surgical pathology 1999;23(7):849-53.
1999: Fioretos T; Strömbeck B; Sandberg T; Johansson B; Billström R; Borg A; Nilsson P G; Van Den Berghe H; Hagemeijer A; Mitelman F; Höglund M
Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations.
Blood 1999;94(1):225-32.
1999: Sciot R; Rosai J; Dal Cin P; de Wever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rydholm A; Tallini G; van den Berghe H; Vanni R; Willén H
Analysis of 35 cases of localized and diffuse tenosynovial giant cell tumor: a report from the Chromosomes and Morphology (CHAMP) study group.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 1999;12(6):576-9.
1999: Sciot R; Samson I; van den Berghe H; Van Damme B; Dal Cin P
Collagenous fibroma (desmoplastic fibroblastoma): genetic link with fibroma of tendon sheath?
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 1999;12(6):565-8.
1999: Dierlamm J; Baens M; Wlodarska I; Stefanova-Ouzounova M; Hernandez J M; Hossfeld D K; De Wolf-Peeters C; Hagemeijer A; Van den Berghe H; Marynen P
The apoptosis inhibitor gene API2 and a novel 18q gene, MLT, are recurrently rearranged in the t(11;18)(q21;q21) associated with mucosa-associated lymphoid tissue lymphomas.
Blood 1999;93(11):3601-9.
1999: Gisselsson D; Höglund M; Mertens F; Johansson B; Dal Cin P; Van den Berghe H; Earnshaw W C; Mitelman F; Mandahl N
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells.
Human genetics 1999;104(4):315-25.
1999: Van den Berghe I; Dal Cin P; Sciot R; Vanvuchelen J; Michielssen P; Hagemeijer A; De Baene L; Van den Berghe H
Translocation (4;8) as a primary chromosome change in a hydropic leiomyoma.
Histopathology 1999;34(4):378.
1999: Falzetti D; Vermeesch J R; Hood T L; Nacheva E P; Matteucci C; Martelli M F; Van den Berghe H; Marynen P; Mecucci C
Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH study.
Leukemia research 1999;23(4):407-13.
1999: Falzetti D; Crescenzi B; Matteuci C; Falini B; Martelli M F; Van Den Berghe H; Mecucci C
Genomic instability and recurrent breakpoints are main cytogenetic findings in Hodgkin's disease.
Haematologica 1999;84(4):298-305.
1999: Kazmierczak B; Dal Cin P; Meyer-Bolte K; Van den Berghe H; Bullerdiek J
HMG1 is not rearranged by 13q12 aberrations in lipomas.
Genes, chromosomes & cancer 1999;24(3):290-2.
1999: Dal Cin P; Fusco A; Belge G; Chiappetta G; Fedele M; Pauwels P; Bullerdiek J; Van den Berghe H
Involvement of the HMGI(Y) gene in a microfollicular adenoma of the thyroid.
Genes, chromosomes & cancer 1999;24(3):286-9.
1999: Wlodarska I; Selleri L; La Starza R; Paternotte C; Evans G A; Boogaerts M; Van den Berghe H; Mecucci C
Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation.
Genes, chromosomes & cancer 1999;24(3):199-206.
1999: Polito P; Dal Cin P; Sciot R; Brock P; Van Eyken P; Van den Berghe H
Embryonal rhabdomyosarcoma with only numerical chromosome changes. Case report and review of the literature.
Cancer genetics and cytogenetics 1999;109(2):161-5.
1999: Sciot R; Dal Cin P; Samson I; van den Berghe H; Van Damme B
Clonal chromosomal changes in juxta-articular myxoma.
Virchows Archiv : an international journal of pathology 1999;434(2):177-80.
1999: Dal Cin P; Pauwels P; Poldermans L J; Sciot R; Van den Berghe H
Clonal chromosome abnormalities in a so-called Dupuytren's subungual exostosis.
Genes, chromosomes & cancer 1999;24(2):162-4.
1999: Dal Cin P; De Smet L; Sciot R; Van Damme B; Van den Berghe H
Trisomy 7 and trisomy 8 in dividing and non-dividing tumor cells in Dupuytren's disease.
Cancer genetics and cytogenetics 1999;108(2):137-40.
1999: Polito P; Dal Cin P; Kazmierczak B; Rogalla P; Bullerdiek J; Van den Berghe H
Deletion of HMG17 in uterine leiomyomas with ring chromosome 1.
Cancer genetics and cytogenetics 1999;108(2):107-9.
1999: Aventín A; La Starza R; Martínez C; Wlodarska I; Boogaerts M; Van den Berghe H; Mecucci C
Involvement of MLL gene in a t(10;11)(q22;q23) and a t(8;11)(q24;q23) identified by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1999;108(1):48-52.
1998: Van den Berghe H; Dal Cin P
Some genetic aspects of ovarian tumors.
European journal of obstetrics, gynecology, and reproductive biology 1998;81(2):283-7.
1998: Kazmierczak B; Dal Cin P; Wanschura S; Borrmann L; Fusco A; Van den Berghe H; Bullerdiek J
HMGIY is the target of 6p21.3 rearrangements in various benign mesenchymal tumors.
Genes, chromosomes & cancer 1998;23(4):279-85.
1998: Wlodarska I; De Wolf-Peeters C; Falini B; Verhoef G; Morris S W; Hagemeijer A; Van den Berghe H
The cryptic inv(2)(p23q35) defines a new molecular genetic subtype of ALK-positive anaplastic large-cell lymphoma.
Blood 1998;92(8):2688-95.
1998: La Starza R; Wlodarska I; Matteucci C; Falzetti D; Baens M; Martelli M F; Van den Berghe H; Marynen P; Mecucci C
Rearrangement between the MYH11 gene at 16p13 and D12S158 at 12p13 in a case of acute myeloid leukemia M1 (AML-M1).
Genes, chromosomes & cancer 1998;23(1):10-5.
1998: Polito P; Dal Cin P; Pauwels P; Christiaens M; Van den Berghe I; Moerman P; Vrints L; Van den Berghe H
An important subgroup of phyllodes tumors of the breast is characterized by rearrangements of chromosomes 1q and 10q.
Oncology reports 1998;5(5):1099-102.
1998: Sciot R; Dal Cin P; Bellemans J; Samson I; Van den Berghe H; Van Damme B
Synovial chondromatosis: clonal chromosome changes provide further evidence for a neoplastic disorder.
Virchows Archiv : an international journal of pathology 1998;433(2):189-91.
1998: La Starza R; Matteucci C; Crescenzi B; Criel A; Selleslag D; Martelli M F; Van den Berghe H; Mecucci C
Trisomy 6 is the hallmark of a dysplastic clone in bone marrow aplasia.
Cancer genetics and cytogenetics 1998;105(1):55-9.
1998: Jehaes E; Decorte R; Peneau A; Petrie J H; Boiry P A; Gilissen A; Moisan J P; Van den Berghe H; Pascal O; Cassiman J J
Mitochondrial DNA analysis on remains of a putative son of Louis XVI, King of France and Marie-Antoinette.
European journal of human genetics : EJHG 1998;6(4):383-95.
1998: Dal Cin P; Timmerman D; Van den Berghe I; Wanschura S; Kazmierczak B; Vergote I; Deprest J; Neven P; Moerman P; Bullerdiek J; Van den Berghe H
Genomic changes in endometrial polyps associated with tamoxifen show no evidence for its action as an external carcinogen.
Cancer research 1998;58(11):2278-81.
1998: Dal Cin P; Wanschura S; Kazmierczak B; Tallini G; Dei Tos A; Bullerdiek J; Van den Berghe I; Moerman P; Van den Berghe H
Amplification and expression of the HMGIC gene in a benign endometrial polyp.
Genes, chromosomes & cancer 1998;22(2):95-9.
1998: Dierlamm J; Stul M; Vranckx H; Michaux L; Weghuis D E; Speleman F; Selleslag D; Kramer M H; Noens L A; Cassiman J J; Van den Berghe H; Hagemeijer A
FISH identifies inv(16)(p13q22) masked by translocations in three cases of acute myeloid leukemia.
Genes, chromosomes & cancer 1998;22(2):87-94.
1998: Dal Cin P; Sciot R; Fletcher C D; Samson I; De Vos R; Mandahl N; Willén H; Larsson O; Van den Berghe H
Inflammatory leiomyosarcoma may be characterized by specific near-haploid chromosome changes.
The Journal of pathology 1998;185(1):112-5.
1998: Michaux L; Dierlamm J; Wlodarska L; Criel A; Louwagie A; Ferrant A; Hagemeijer A; Van den Berghe H
Trisomy 3q11-q29 is recurrently observed in B-cell non-Hodgkin's lymphomas associated with cold agglutinin syndrome.
Annals of hematology 1998;76(5):201-4.
1998: Dal Cin P; Sciot R; De Smet L; Van den Berghe H
Translocation 2;11 in a fibroma of tendon sheath.
Histopathology 1998;32(5):433-5.
1998: Dal Cin P; Lipcsei G; Hermand G; Boniver J; Van den Berghe H
Congenital mesoblastic nephroma and trisomy 11.
Cancer genetics and cytogenetics 1998;103(1):68-70.
1998: Mertens F; Fletcher C D; Dal Cin P; De Wever I; Mandahl N; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Vanni R; Willén H
Cytogenetic analysis of 46 pleomorphic soft tissue sarcomas and correlation with morphologic and clinical features: a report of the CHAMP Study Group. Chromosomes and MorPhology.
Genes, chromosomes & cancer 1998;22(1):16-25.
1998: Willén H; Akerman M; Dal Cin P; De Wever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Vanni R
Comparison of chromosomal patterns with clinical features in 165 lipomas: a report of the CHAMP study group.
Cancer genetics and cytogenetics 1998;102(1):46-9.
1998: Dal Cin P; Pauwels P; Moerman P; Qi H; Van Den Berghe H
Hyperdiploidy in benign breast lesions.
Cancer genetics and cytogenetics 1998;101(2):162-3.
1998: Kazmierczak B; Dal Cin P; Wanschura S; Bartnitzke S; Van den Berghe H; Bullerdiek J
Cloning and molecular characterization of part of a new gene fused to HMGIC in mesenchymal tumors.
The American journal of pathology 1998;152(2):431-5.
1998: Dal Cin P; Stas M; Sciot R; De Wever I; Van Damme B; Van den Berghe H
Translocation (X;1) reveals metastasis 31 years after renal cell carcinoma.
Cancer genetics and cytogenetics 1998;101(1):58-61.
1998: Wlodarska I; La Starza R; Baens M; Dierlamm J; Uyttebroeck A; Selleslag D; Francine A; Mecucci C; Hagemeijer A; Van den Berghe H; Marynen P
Fluorescence in situ hybridization characterization of new translocations involving TEL (ETV6) in a wide spectrum of hematologic malignancies.
Blood 1998;91(4):1399-406.
1998: Dal Cin P; Dei Tos A P; Qi H; Giannini C; Furlanetto A; Longatti P L; Marynen P; Van den Berghe H
Immature teratoma of the pineal gland with isochromosome 12p.
Acta neuropathologica 1998;95(1):107-10.
1998: Bonato M; Pittaluga S; Tierens A; Criel A; Verhoef G; Wlodarska I; Vanutysel L; Michaux L; Vandekerckhove P; Van den Berghe H; De Wolf-Peeters C
Lymph node histology in typical and atypical chronic lymphocytic leukemia.
The American journal of surgical pathology 1998;22(1):49-56.
1998: La Starza R; Wlodarska I; Aventin A; Falzetti D; Crescenzi B; Martelli M F; Van den Berghe H; Mecucci C
Molecular delineation of 13q deletion boundaries in 20 patients with myeloid malignancies.
Blood 1998;91(1):231-7.
1997: Dal Cin P; Sciot R; Van Poppel H; Baert L; Van Damme B; Van den Berghe H
Chromosome analysis in angiomyolipoma.
Cancer genetics and cytogenetics 1997;99(2):132-4.
1997: Dal Cin P; Qi H; Pauwels P; Backx C; Van den Berghe H
Monosomy 22 in a fibrothecoma.
Cancer genetics and cytogenetics 1997;99(2):129-31.
1997: Decruyenaere M; Evers-Kiebooms G; Boogaerts A; Cloostermans T; Cassiman J J; Demyttenaere K; Dom R; Fryns J P; Van den Berghe H
Non-participation in predictive testing for Huntington's disease: individual decision-making, personality and avoidant behaviour in the family.
European journal of human genetics : EJHG 1997;5(6):351-63.
1997: Dierlamm J; Wlodarska I; Michaux L; Vermeesch J R; Meeus P; Stul M; Criel A; Verhoef G; Thomas J; Delannoy A; Louwagie A; Cassiman J J; Mecucci C; Hagemeijer A; Van den Berghe H
FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12.
Genes, chromosomes & cancer 1997;20(2):155-66.
1997: Wlodarska I; Pittaluga S; Stul M; Martiat P; Dierlamm J; Michaux L; De Wolf-Peeters C; Cassiman J J; Mecucci C; Van den Berghe H
Philadelphia-like translocation t(9;22)(q34;q11) found in a follicular lymphoma involving not BCR and ABL but IGL-mediated rearrangement of an unknown gene on 9q34.
Genes, chromosomes & cancer 1997;20(2):113-9.
1997: Peeters P; Raynaud S D; Cools J; Wlodarska I; Grosgeorge J; Philip P; Monpoux F; Van Rompaey L; Baens M; Van den Berghe H; Marynen P
Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia.
Blood 1997;90(7):2535-40.
1997: Dal Cin P; Sciot R; Polito P; Stas M; de Wever I; Cornelis A; Van den Berghe H
Lesions of 13q may occur independently of deletion of 16q in spindle cell/pleomorphic lipomas.
Histopathology 1997;31(3):222-5.
1997: Dierlamm J; Pittaluga S; Stul M; Wlodarska I; Michaux L; Thomas J; Verhoef G; Verhest A; Depardieu C; Cassiman J J; Hagemeijer A; De Wolf-Peeters C; Van den Berghe H
BCL6 gene rearrangements also occur in marginal zone B-cell lymphoma.
British journal of haematology 1997;98(3):719-25.
1997: Dal Cin P; Wanschura S; Christiaens M R; Van den Berghe I; Moerman P; Polito P; Kazmierczak B; Bullerdiek J; Van den Berghe H
Hamartoma of the breast with involvement of 6p21 and rearrangement of HMGIY.
Genes, chromosomes & cancer 1997;20(1):90-2.
1997: Dal Cin P; Polito P; Van Eyken P; Sciot R; Hernandez J M; Garcia J L; Van den Berghe H
Anomalies of chromosomes 17 and 22 in giant cell fibroblastoma.
Cancer genetics and cytogenetics 1997;97(2):165-6.
1997: de Wolf-Peeters C; Pittaluga S; Dierlamm J; Wlodarska I; Van Den Berghe H
Marginal zone B-cell lymphomas including mucosa-associated lymphoid tissue type lymphoma (MALT), monocytoid B-cell lymphoma and splenic marginal zone cell lymphoma and their relation to the reactive marginal zone.
Leukemia & lymphoma 1997;26(5-6):467-78.
1997: Pittaluga S; Wlodarska I; Pulford K; Campo E; Morris S W; Van den Berghe H; De Wolf-Peeters C
The monoclonal antibody ALK1 identifies a distinct morphological subtype of anaplastic large cell lymphoma associated with 2p23/ALK rearrangements.
The American journal of pathology 1997;151(2):343-51.
1997: Tallini G; Dal Cin P; Rhoden K J; Chiapetta G; Manfioletti G; Giancotti V; Fusco A; Van den Berghe H; Sciot R
Expression of HMGI-C and HMGI(Y) in ordinary lipoma and atypical lipomatous tumors: immunohistochemical reactivity correlates with karyotypic alterations.
The American journal of pathology 1997;151(1):37-43.
1997: Dierlamm J; Rosenberg C; Stul M; Pittaluga S; Wlodarska I; Michaux L; Dehaen M; Verhoef G; Thomas J; de Kelver W; Bakker-Schut T; Cassiman J J; Raap A K; De Wolf-Peeters C; Van den Berghe H; Hagemeijer A
Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(5):747-58.
1997: Criel A; Verhoef G; Vlietinck R; Mecucci C; Billiet J; Michaux L; Meeus P; Louwagie A; Van Orshoven A; Van Hoof A; Boogaerts M; Van den Berghe H; De Wolf-Peeters C
Further characterization of morphologically defined typical and atypical CLL: a clinical, immunophenotypic, cytogenetic and prognostic study on 390 cases.
British journal of haematology 1997;97(2):383-91.
1997: Dal Cin P; Van den Berghe H
Ten years of the cytogenetics of soft tissue tumors.
Cancer genetics and cytogenetics 1997;95(1):59-66.
1997: Sciot R; Akerman M; Dal Cin P; De Wever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Tallini G; Van den Berghe H; Vanni R; Willen H
Cytogenetic analysis of subcutaneous angiolipoma: further evidence supporting its difference from ordinary pure lipomas: a report of the CHAMP Study Group.
The American journal of surgical pathology 1997;21(4):441-4.
1997: Wanschura S; Dal Cin P; Kazmierczak B; Bartnitzke S; Van den Berghe H; Bullerdiek J
Hidden paracentric inversions of chromosome arm 12q affecting the HMGIC gene.
Genes, chromosomes & cancer 1997;18(4):322-3.
1997: Dierlamm J; Michaux L; Criel A; Wlodarska I; Van den Berghe H; Hossfeld D K
Genetic abnormalities in chronic lymphocytic leukemia and their clinical and prognostic implications.
Cancer genetics and cytogenetics 1997;94(1):27-35.
1997: Van den Berghe H; Michaux L
5q-, twenty-five years later: a synopsis.
Cancer genetics and cytogenetics 1997;94(1):1-7.
1997: Wlodarska I; Aventín A; Inglés-Esteve J; Falzetti D; Criel A; Cassiman J J; Mecucci C; Van den Berghe H; Marynen P
A new subtype of pre-B acute lymphoblastic leukemia with t(5;12)(q31q33;p12), molecularly and cytogenetically distinct from t(5;12) in chronic myelomonocytic leukemia.
Blood 1997;89(5):1716-22.
1997: Hernández J M; Schoenmakers E F; Dal Cin P; Michaux L; Van de Ven W J; Van den Berghe H
Molecular delineation of the commonly deleted segment in mature B-cell lymphoid neoplasias with deletion of 7q.
Genes, chromosomes & cancer 1997;18(2):147-50.
1997: Dal Cin P; Qi H; Sciot R; Van den Berghe H
Involvement of chromosomes 6 and 11 in a soft tissue chondroma.
Cancer genetics and cytogenetics 1997;93(2):177-8.
1997: Hernandez J M; Mecucci C; Michaux L; Criel A; Stul M; Meeus P; Wlodarska I; Van Orshoven A; Cassiman J J; De Wolf-Peeters C; Van den Berghe H
del(7q) in chronic B-cell lymphoid malignancies.
Cancer genetics and cytogenetics 1997;93(2):147-51.
1997: Peeters P; Wlodarska I; Baens M; Criel A; Selleslag D; Hagemeijer A; Van den Berghe H; Marynen P
Fusion of ETV6 to MDS1/EVI1 as a result of t(3;12)(q26;p13) in myeloproliferative disorders.
Cancer research 1997;57(4):564-9.
1997: Vermeesch J R; Petit P; Kermouni A; Renauld J C; Van Den Berghe H; Marynen P
The IL-9 receptor gene, located in the Xq/Yq pseudoautosomal region, has an autosomal origin, escapes X inactivation and is expressed from the Y.
Human molecular genetics 1997;6(1):1-8.
1996: Fryns J P; Legius E; Demaerel P; van den Berghe H
Congenital scalp defect, distal limb reduction anomalies, right spastic hemiplegia and hypoplasia of the left arteria cerebri media. Further evidence that interruption of early embryonic blood supply may result in Adams-Oliver (plus) syndrome.
Clinical genetics 1996;50(6):505-9.
1996: Qi H; Dal Cin P; Hernández J M; Garcia J L; Sciot R; Fletcher C; Van Eyken P; De Wever I; Van den Berghe H
Trisomies 8 and 20 in desmoid tumors.
Cancer genetics and cytogenetics 1996;92(2):147-9.
1996: Cuneo A; Ferrant A; Michaux J L; Bosly A; Chatelain B; Stul M; Dal Cin P; Dierlamm J; Cassiman J J; Hossfeld D K; Castoldi G; Van den Berghe H
Cytogenetic and clinicobiological features of acute leukemia with stem cell phenotype: study of nine cases.
Cancer genetics and cytogenetics 1996;92(1):31-6.
1996: Wlodarska I; Mecucci C; Baens M; Marynen P; van den Berghe H
ETV6 gene rearrangements in hematopoietic malignant disorders.
Leukemia & lymphoma 1996;23(3-4):287-95.
1996: Evers-Kiebooms G; Fryns J P; Demyttenaere K; Decruyenaere M; Boogaerts A; Cloostermans T; Cassiman J J; Dom R; Van den Berghe H
Predictive and preimplantation genetic testing for Huntington's disease and other late onset dominant disorders: not in conflict but complementary.
Clinical genetics 1996;50(4):275-6.
1996: Fryns J P; Kleczkowska A; Timmermans J; van den Berghe H
The Floating-Harbor syndrome: two affected siblings in a family.
Clinical genetics 1996;50(4):217-9.
1996: Dal Cin P; Van Poppel H; Sciot R; De Vos R; Van Damme B; Baert L; Van den Berghe H
The t(1;12)(p36;q13) in a renal oncocytoma.
Genes, chromosomes & cancer 1996;17(2):136-9.
1996: Dal Cin P; Marynen P; Moerman P; Vergot I; Van den Berghe H
Ovarian germ cell tumor with chromosome 12 anomaly but without i(12p).
Cancer genetics and cytogenetics 1996;91(1):61-4.
1996: Rosai J; Akerman M; Dal Cin P; DeWever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Van de Ven W; Vanni R; Willen H
Combined morphologic and karyotypic study of 59 atypical lipomatous tumors. Evaluation of their relationship and differential diagnosis with other adipose tissue tumors (a report of the CHAMP Study Group).
The American journal of surgical pathology 1996;20(10):1182-9.
1996: Cuneo A; Ferrant A; Michaux J L; Demuynck H; Boogaerts M; Louwagie A; Doyen C; Stul M; Cassiman J J; Dal Cin P; Castoldi G; Van den Berghe H
Philadelphia chromosome-positive acute myeloid leukemia: cytoimmunologic and cytogenetic features.
Haematologica 1996;81(5):423-7.
1996: Decruyenaere M; Evers-Kiebooms G; Boogaerts A; Cassiman J J; Cloostermans T; Demyttenaere K; Dom R; Fryns J P; Van den Berghe H
Prediction of psychological functioning one year after the predictive test for Huntington's disease and impact of the test result on reproductive decision making.
Journal of medical genetics 1996;33(9):737-43.
1996: Mandahl N; Akerman M; Aman P; Dal Cin P; De Wever I; Fletcher C D; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Van de Ven W; Vanni R; Willén H
Duplication of chromosome segment 12q15-24 is associated with atypical lipomatous tumors: a report of the CHAMP collaborative study group. CHromosomes And MorPhology.
International journal of cancer. Journal international du cancer 1996;67(5):632-5.
1996: Tallini G; Akerman M; Dal Cin P; De Wever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Van den Berghe H; Van den Ven W; Vanni R; Willen H
Combined morphologic and karyotypic study of 28 myxoid liposarcomas. Implications for a revised morphologic typing, (a report from the CHAMP Group).
The American journal of surgical pathology 1996;20(9):1047-55.
1996: Brosens I; Johannisson E; Dal Cin P; Deprest J; Van den Berghe H
Analysis of the karyotype and desoxyribonucleic acid content of uterine myomas in premenopausal, menopausal, and gonadotropin-releasing hormone agonist-treated females.
Fertility and sterility 1996;66(3):376-9.
1996: Dierlamm J; Wlodarska I; Michaux L; La Starza R; Zeller W; Mecucci C; Van den Berghe H
Successful use of the same slide for consecutive fluorescence in situ hybridization experiments.
Genes, chromosomes & cancer 1996;16(4):261-4.
1996: Petit P; Schmit J; Van den Berghe H; Fryns J P
On two patients with and without the classical Wolf-Hirschhorn syndrome (WHS) sharing the same chromosome 4p16.3 specific probe deletion: evidence of a contiguous gene deletion syndrome.
Clinical genetics 1996;50(1):19-22.
1996: Pauwels P; Dal Cin P; Van de Moosdijk C N; Vrints L; Sciot R; Van den Berghe H
Cytogenetics revealing the diagnosis in a metastatic endometrial stromal sarcoma.
Histopathology 1996;29(1):84-7.
1996: Dal Cin P; De Wolf-Peeters C; Deneffe G; Fryns J P; Van den Berghe H
Thymoma with a t(15;22)(p11;q11).
Cancer genetics and cytogenetics 1996;89(2):181-3.
1996: Dierlamm J; Michaux L; Kröger N; Wlodarska I; Martiat P; Zeller W; Seeger D; Mecucci C; van den Berghe H; Hossfeld D K
ider(9)(q10)t(9;22)(q34;q11) is a recurrent chromosomal abnormality in acute lymphoblastic leukemia and lymphatic blastic phase of chronic myelogenous leukemia.
Cancer genetics and cytogenetics 1996;89(2):109-13.
1996: Dal Cin P; van Poppel H; van Damme B; Baert L; Van den Berghe H
Cytogenetic investigation of synchronous bilateral renal tumors.
Cancer genetics and cytogenetics 1996;89(1):57-60.
1996: Pittaluga S; Ayoubi T A; Wlodarska I; Stul M; Cassiman J J; Mecucci C; Van Den Berghe H; Van De Ven W J; De Wolf-Peeters C
BCL-6 expression in reactive lymphoid tissue and in B-cell non-Hodgkin's lymphomas.
The Journal of pathology 1996;179(2):145-50.
1996: Wlodarska I; Baens M; Peeters P; Aerssens J; Mecucci C; Brock P; Marynen P; Van den Berghe H
Biallelic alterations of both ETV6 and CDKN1B genes in a t(12;21) childhood acute lymphoblastic leukemia case.
Cancer research 1996;56(11):2655-61.
1996: Cuneo A; Castoldi G; Michaux J L; Ferrant A; Chatelain B; Louwagie A; St Jan A Z; Boogaerts M; Dal Cin P; Van den Berghe H
Differences in the chromosomal profile of AML-M0 versus AML-M1: response.
Blood 1996;87(12):5381-2.
1996: Dal Cin P; Moerman P; Christiaens M R; Van den Berghe H
Observation of a deletion of the long arm of chromosome 6 in benign fibrocystic disease of the breast constitutes a challenging problem.
Genes, chromosomes & cancer 1996;16(1):68-71.
1996: Fryns J P; Legius E; Devriendt K; Meire F; Standaert L; Baten E; Van den Berghe H
Cohen syndrome: the clinical symptoms and stigmata at a young age.
Clinical genetics 1996;49(5):237-41.
1996: Denayer L; Welkenhuysen M; Evers-Kiebooms G; Cassiman J J; Van den Berghe H
The CF carrier status is not associated with a diminished self-concept or increased anxiety: results of psychometric testing after at least 1 year.
Clinical genetics 1996;49(5):232-6.
1996: Demuynck H; Verhoef G E; Zachee P; Emonds M P; van der Schueren E; van den Berghe H; Vandenberghe P; Casteels-Van Daele M; Boogaerts M A
Treatment of patients with myelodysplastic syndromes with allogeneic bone marrow transplantation from genotypically HLA-identical sibling and alternative donors.
Bone marrow transplantation 1996;17(5):745-51.
1996: Criel A; Pittaluga S; Verhoef G; Wlodarska I; Meeus P; Mecucci C; Van Orshoven A; Van den Berghe H; Boogaerts M; De Wolf-Peeters C
Small B cell NHL and their leukemic counterpart: differences in subtyping and assessment of leukemic spread.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(5):848-53.
1996: Michaux L; Dierlamm J; Mecucci C; Meeus P; Ameye G; Libouton J M; Verhoef G; Ferrant A; Louwagie A; Verellen-Dumoulin C; Van Den Berghe H
Dicentric (1;15) in myeloid disorders.
Cancer genetics and cytogenetics 1996;88(1):86-9.
1996: Dal Cin P; Pauwels P; Sciot R; Van den Berghe H
Multiple chromosome rearrangements in a fibrosarcoma.
Cancer genetics and cytogenetics 1996;87(2):176-8.
1996: Dierlamm J; Michaux L; Wlodarska I; Pittaluga S; Zeller W; Stul M; Criel A; Thomas J; Boogaerts M; Delaere P; Cassiman J J; de Wolf-Peeters C; Mecucci C; Van den Berghe H
Trisomy 3 in marginal zone B-cell lymphoma: a study based on cytogenetic analysis and fluorescence in situ hybridization.
British journal of haematology 1996;93(1):242-9.
1996: Steinfeld R; Van Den Berghe H; David G
Stimulation of fibroblast growth factor receptor-1 occupancy and signaling by cell surface-associated syndecans and glypican.
The Journal of cell biology 1996;133(2):405-16.
1996: Dal Cin P; Scoit R; De Smet L; Van Damme B; Van Den Berghe H
A new cytogenetic subgroup in tenosynovial giant cell tumors (nodular tenosynovitis) is characterized by involvement of 16q24.
Cancer genetics and cytogenetics 1996;87(1):85-7.
1996: Qi H; Dal Cin P; Van de Voorde W; Elgamal A A; Van Poppel H; Baert L; Van Den Berghe H
del(1)(q12) in adenocarcinomas of the prostate.
Cancer genetics and cytogenetics 1996;87(1):79-81.
1996: Velloso E R; Michaux L; Ferrant A; Hernandez J M; Meeus P; Dierlamm J; Criel A; Louwagie A; Verhoef G; Boogaerts M; Michaux J L; Bosly A; Mecucci C; Van den Berghe H
Deletions of the long arm of chromosome 7 in myeloid disorders: loss of band 7q32 implies worst prognosis.
British journal of haematology 1996;92(3):574-81.
1996: Mertens G; Van der Schueren B; van den Berghe H; David G
Heparan sulfate expression in polarized epithelial cells: the apical sorting of glypican (GPI-anchored proteoglycan) is inversely related to its heparan sulfate content.
The Journal of cell biology 1996;132(3):487-97.
1996: Demuynck H; Delforge M; Verhoef G E; Zachee P; Vandenberghe P; Van den Berghe H; Boogaerts M A
Feasibility of peripheral blood progenitor cell harvest and transplantation in patients with poor-risk myelodysplastic syndromes.
British journal of haematology 1996;92(2):351-9.
1996: Fletcher C D; Akerman M; Dal Cin P; de Wever I; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; van den Berghe H; van de Ven W; Vanni R; Willen H
Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
The American journal of pathology 1996;148(2):623-30.
1996: Pittaluga S; Verhoef G; Criel A; Wlodarska I; Dierlamm J; Mecucci C; Van den Berghe H; De Wolf-Peeters C
"Small" B-cell non-Hodgkin's lymphomas with splenomegaly at presentation are either mantle cell lymphoma or marginal zone cell lymphoma. A study based on histology, cytology, immunohistochemistry, and cytogenetic analysis.
The American journal of surgical pathology 1996;20(2):211-23.
1996: Dal Cin P; Sciot R; de Wever I; Brock P; Casteels-Van Daele M; Van Damme B; Van Den Berghe H
Cytogenetic and immunohistochemical evidence that giant cell fibroblastoma is related to dermatofibrosarcoma protuberans.
Genes, chromosomes & cancer 1996;15(1):73-5.
1996: Michaux L; Mecucci C; Stul M; Wlodarska I; Hernandez J M; Meeus P; Michaux J L; Scheiff J M; Noël H; Louwagie A; Criel A; Boogaerts M; Van Orshoven A; Cassiman J J; Van Den Berghe H
BCL3 rearrangement and t(14;19)(q32;q13) in lymphoproliferative disorders.
Genes, chromosomes & cancer 1996;15(1):38-47.
1996: Meulemans W J; Lewis C M; Boomsma D I; Derom C A; Van den Berghe H; Orlebeke J F; Vlietinck R F; Derom R M
Genetic modelling of dizygotic twinning in pedigrees of spontaneous dizygotic twins.
American journal of medical genetics 1996;61(3):258-63.
1996: Devriendt K; Van den Berghe H; Fryns J P
Alopecia-mental retardation syndrome associated with convulsions and hypergonadotropic hypogonadism.
Clinical genetics 1996;49(1):6-9.
1996: Fryns J P; Lorenzetti M E; Maroteaux P; Van den Berghe H
Micromelic dwarfism with cone epiphyses, metaphyseal dysplasia, and vertebral segmentation defects.
American journal of medical genetics 1996;61(2):164-7.
1996: Devriendt K; van den Oord J; De Vos R; Van den Berghe H; Fryns J P
Ichthyosis-characteristic appearance-mental retardation syndrome with distinct histological skin abnormalities.
American journal of medical genetics 1996;61(2):127-30.
1996: Dal Cin P; Sciot R; Fletcher C D; Hilliker C; De Wever I; Van Damme B; Van den Berghe H
Trisomy 21 in solitary fibrous tumor.
Cancer genetics and cytogenetics 1996;86(1):58-60.
1996: Wanschura S; Belge G; Stenman G; Kools P; Dal Cin P; Schoenmakers E; Huysmans C; Van den Berghe H; Bartnitzke S; Van de Ven W J; Bullerdiek J
Mapping of the translocation breakpoints of primary pleomorphic adenomas and lipomas within a common region of chromosome 12.
Cancer genetics and cytogenetics 1996;86(1):39-45.
1996: Dierlamm J; Pittaluga S; Wlodarska I; Stul M; Thomas J; Boogaerts M; Michaux L; Driessen A; Mecucci C; Cassiman J J; De Wolf-Peeters C; Van den Berghe H
Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features.
Blood 1996;87(1):299-307.
1996: Van den Berghe H
[Possibilities and problems created by the development in human genetics]
Verhandelingen - Koninklijke Academie voor Geneeskunde van België 1996;58(4):339-56; discussion 356-8.
1996: Wlodarska I; Marynen P; La Starza R; Mecucci C; Van den Berghe H
The ETV6, CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberration in different hematological malignancies.
Cytogenetics and cell genetics 1996;72(2-3):229-35.
1996: Fryns J P; Bonhomme A; Van den Berghe H
Nager acrofacial dysostosis. An adult male with severe neurological deficit.
Genetic counseling (Geneva, Switzerland) 1996;7(2):147-51.
1996: Smeets E; Fryns J P; Van den Berghe H
The Floating-Harbor syndrome: report of another patient and differential diagnosis with Shprintzen syndrome.
Genetic counseling (Geneva, Switzerland) 1996;7(2):143-6.
1996: Welkenhuysen M; Evers-Kiebooms G; Decruyenaere M; Van den Berghe H; Bande-Knops J; Van Gerven V
Adolescents' attitude towards carrier testing for cystic fibrosis and its relative stability over time.
European journal of human genetics : EJHG 1996;4(1):52-62.
1996: Vermeesch J R; De Meurichy W; Van Den Berghe H; Marynen P; Petit P
Differences in the distribution and nature of the interstitial telomeric (TTAGGG)n sequences in the chromosomes of the Giraffidae, okapai (Okapia johnstoni), and giraffe (Giraffa camelopardalis): evidence for ancestral telomeres at the okapi polymorphic rob(5;26) fusion site.
Cytogenetics and cell genetics 1996;72(4):310-5.
1996: Kas K; Wlodarska I; Meyen E; Van den Berghe H; Van de Ven W J
Assignment of the gene encoding human Krüppel-related zinc finger protein 4 (GLI4) to 8q24.3 by fluorescent in situ hybridization.
Cytogenetics and cell genetics 1996;72(4):297-8.
1995: Dierlamm J; Michaux L; Criel A; Wlodarska I; Zeller W; Louwagie A; Michaux J L; Mecucci C; Van den Berghe H
Isodicentric (X)(q13) in haematological malignancies: presentation of five new cases, application of fluorescence in situ hybridization (FISH) and review of the literature.
British journal of haematology 1995;91(4):885-91.
1995: De Strooper B; Craessaerts K; Van Leuven F; Van Den Berghe H
Exchanging the extracellular domain of amyloid precursor protein for horseradish peroxidase does not interfere with alpha-secretase cleavage of the beta-amyloid region, but randomizes secretion in Madin-Darby canine kidney cells.
The Journal of biological chemistry 1995;270(51):30310-4.
1995: Delforge M; Demuynck H; Vandenberghe P; Verhoef G; Zachée P; van Duppen V; Marijnen P; Van den Berghe H; Boogaerts M A
Polyclonal primitive hematopoietic progenitors can be detected in mobilized peripheral blood from patients with high-risk myelodysplastic syndromes.
Blood 1995;86(10):3660-7.
1995: Van Rompaey L; Proost P; Van den Berghe H; Marynen P
Design of a new protease inhibitor by the manipulation of the bait region of alpha 2-macroglobulin: inhibition of the tobacco etch virus protease by mutant alpha 2-macroglobulin.
The Biochemical journal 1995;312 ( Pt 1)():191-5.
1995: Van Rompaey L; Van den Berghe H; Marynen P
Synthesis of a Cys949Tyr alpha 2-macroglobulin thiol ester mutant: co-transfection with wild-type alpha 2-macroglobulin in an episomal expression system.
The Biochemical journal 1995;312 ( Pt 1)():183-90.
1995: Sciot R; Dal Cin P; Fletcher C D; De Wever I; De Vos R; Van Damme B; Van den Berghe H
Monosomy 22 in a malignant peripheral nerve sheath tumour of the kidney in childhood: a genetic link with other malignant paediatric renal neoplasms?
Histopathology 1995;27(4):373-6.
1995: Schoenmakers E F; Geurts J M; Kools P F; Mols R; Huysmans C; Bullerdiek J; Van den Berghe H; Van de Ven W J
A 6-Mb yeast artificial chromosome contig and long-range physical map encompassing the region on chromosome 12q15 frequently rearranged in a variety of benign solid tumors.
Genomics 1995;29(3):665-78.
1995: Decruyenaere M; Evers-Kiebooms G; Welkenhuysen M; Bande-Knops J; Van Gerven V; Van den Berghe H
Adolescents' opinions about genetic risk information, prenatal diagnosis, and pregnancy termination.
Journal of medical genetics 1995;32(10):799-804; discussion 805.
1995: Michaux L; Dierlamm J; Wlodarska I; Stul M; Bosly A; Delannoy A; Louwagie A; Mecucci C; Cassiman J J; van den Berghe H
Trisomy 3 is a consistent chromosome change in malignant lymphoproliferative disorders preceded by cold agglutinin disease.
British journal of haematology 1995;91(2):421-4.
1995: Wlodarska I; De Wolf-Peeters C; Michaux L; Mecucci C; Verhoef G; Cassiman J J; Van den Berghe H
A new t(2;5) translocation in a null cell type CD30 positive anaplastic large cell lymphoma case.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(10):1685-8.
1995: Fryns J P; Smeets E; Van den Berghe H
On the nosology of the "primary true microcephaly, chorioretinal dysplasia, lymphoedema" association.
Clinical genetics 1995;48(3):131-3.
1995: Baens M; Aerssens J; van Zand K; Van den Berghe H; Marynen P
Isolation and regional assignment of human chromosome 12p cDNAs.
Genomics 1995;29(1):44-52.
1995: Raeymaekers P; Van Zand K; Jun L; Höglund M; Cassiman J J; Van den Berghe H; Marynen P
A radiation hybrid map with 60 loci covering the entire short arm of chromosome 12.
Genomics 1995;29(1):170-8.
1995: Wlodarska I; Mecucci C; Stul M; Michaux L; Pittaluga S; Hernandez J M; Cassiman J J; De Wolf-Peeters C; Van den Berghe H
Fluorescence in situ hybridization identifies new chromosomal changes involving 3q27 in non-Hodgkin's lymphomas with BCL6/LAZ3 rearrangement.
Genes, chromosomes & cancer 1995;14(1):1-7.
1995: Fryns J P; Legius E; Moerman P; Vandenberghe K; Van den Berghe H
Apparently new "anophthalmia-plus" syndrome in sibs.
American journal of medical genetics 1995;58(2):113-4.
1995: Schoenmakers E F; Wanschura S; Mols R; Bullerdiek J; Van den Berghe H; Van de Ven W J
Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours.
Nature genetics 1995;10(4):436-44.
1995: Meeus P; Stul M S; Mecucci C; Cassiman J J; Van den Berghe H
Molecular breakpoints of t(11;14)(q13;q32) in multiple myeloma.
Cancer genetics and cytogenetics 1995;83(1):25-7.
1995: Umans L; Serneels L; Overbergh L; Lorent K; Van Leuven F; Van den Berghe H
Targeted inactivation of the mouse alpha 2-macroglobulin gene.
The Journal of biological chemistry 1995;270(34):19778-85.
1995: Dal Cin P; Moerman P; Deprest J; Brosens I; Van den Berghe H
A new cytogenetic subgroup in uterine leiomyoma is characterized by a deletion of the long arm of chromosome 3.
Genes, chromosomes & cancer 1995;13(3):219-20.
1995: Michaux L; Wlodarska I; Mecucci C; Hernandez J M; Van Orshoven A; Michaux J L; Van den Berghe H
Characterization by chromosome painting of balanced and unbalanced X chromosome translocations in myelodysplastic syndromes.
Cancer genetics and cytogenetics 1995;82(1):17-22.
1995: Sciot R; Samson I; Dal Cin P; Lateur L; van Damme B; van den Berghe H; Desmet V
Giant cell rich parosteal osteosarcoma.
Histopathology 1995;27(1):51-5.
1995: Dal Cin P; Vanni R; Marras S; Moerman P; Kools P; Andria M; Valdes E; Deprest J; Van de Ven W; Van den Berghe H
Four cytogenetic subgroups can be identified in endometrial polyps.
Cancer research 1995;55(7):1565-8.
1995: Uyttebroeck A; Brock P; De Groote B; Renard M; Dal Cin P; Van den Berghe H; Casteels-Van Daele M
5q- syndrome in a child.
Cancer genetics and cytogenetics 1995;80(2):121-3.
1995: Lorent K; Overbergh L; Moechars D; De Strooper B; Van Leuven F; Van den Berghe H
Expression in mouse embryos and in adult mouse brain of three members of the amyloid precursor protein family, of the alpha-2-macroglobulin receptor/low density lipoprotein receptor-related protein and of its ligands apolipoprotein E, lipoprotein lipase, alpha-2-macroglobulin and the 40,000 molecular weight receptor-associated protein.
Neuroscience 1995;65(4):1009-25.
1995: Van de Ven W J; Schoenmakers E F; Wanschura S; Kazmierczak B; Kools P F; Geurts J M; Bartnitzke S; Van den Berghe H; Bullerdiek J
Molecular characterization of MAR, a multiple aberration region on human chromosome segment 12q13-q15 implicated in various solid tumors.
Genes, chromosomes & cancer 1995;12(4):296-303.
1995: De Strooper B; Craessaerts K; Dewachter I; Moechars D; Greenberg B; Van Leuven F; Van den Berghe H
Basolateral secretion of amyloid precursor protein in Madin-Darby canine kidney cells is disturbed by alterations of intracellular pH and by introducing a mutation associated with familial Alzheimer's disease.
The Journal of biological chemistry 1995;270(8):4058-65.
1995: Kools P F; Wanschura S; Schoenmakers E F; Geurts J M; Mols R; Kazmierczak B; Bullerdiek J; Van den Berghe H; Van de Ven W J
Identification of the chromosome 12 translocation breakpoint region of a pleomorphic salivary gland adenoma with t(1;12)(p22;q15) as the sole cytogenetic abnormality.
Cancer genetics and cytogenetics 1995;79(1):1-7.
1995: De Strooper B; Creemers J W; Moechars D; Huylebroeck D; Van De Ven W J; Van Leuven F; Van den Berghe H
Amyloid precursor protein is not processed by furin, PACE 4, PC1/3, PC2, PC4 and PC5/6 of the furin family of proprotein processing enzymes.
Biochimica et biophysica acta 1995;1246(2):185-8.
1995: Van Leuven F; Hilliker C; Serneels L; Umans L; Overbergh L; De Strooper B; Fryns J P; Van den Berghe H
Cloning, characterization, and chromosomal localization to 4p16 of the human gene (LRPAP1) coding for the alpha 2-macroglobulin receptor-associated protein and structural comparison with the murine gene coding for the 44-kDa heparin-binding protein.
Genomics 1995;25(2):492-500.
1995: Pittaluga S; Wlodarska I; Stul M S; Thomas J; Verhoef G; Cassiman J J; Van den Berghe H; de Wolf-Peeters C
Mantle cell lymphoma: a clinicopathological study of 55 cases.
Histopathology 1995;26(1):17-24.
1995: Decruyenaere M; Evers-Kiebooms G; Boogaerts A; Cassiman J J; Cloostermans T; Demyttenaere K; Dom R; Fryns J P; Van den Berghe H
Predictive testing for Huntington's disease: risk perception, reasons for testing and psychological profile of test applicants.
Genetic counseling (Geneva, Switzerland) 1995;6(1):1-13.
1995: Van Dorpe J; Van Damme S; Jacobs V; Van den Berghe H; Criel A; Michielssen P; Louwagie A
T-lymphoid extramedullary (lymphadenopathic) blast crisis in CML.
Acta clinica Belgica 1995;50(2):121-5.
1995: Aerssens J; Guo C; Vermeesch J; Baens M; Browne D; Litt M; Van Den Berghe H; Marynen P
A physical map of the region spanning the chromosome 12 translocation breakpoint in a mesothelioma with a t(X;12)(q22;p13).
Cytogenetics and cell genetics 1995;71(3):268-75.
1995: Borghgraef M; Swillen A; Van den Berghe H; Fryns J P
Fragile X boys: evolution of the mental age in childhood. Preliminary data on 10 prepubertal boys.
Genetic counseling (Geneva, Switzerland) 1995;6(2):97-101.
1995: Cuneo A; Boogaerts M; Ferrant A; Michaux J L; Bosly A; Louwagie A; Van den Berghe H; Balsamo R; Roberti G; Bardi A
Cytogenetics of hybrid acute leukemias.
Leukemia & lymphoma 1995;18 Suppl 1():19-23.
1994: Dal Cin P; Sciot R; De Wever I; Van Damme B; Van den Berghe H
New discriminative chromosomal marker in adipose tissue tumors. The chromosome 8q11-q13 region in lipoblastoma.
Cancer genetics and cytogenetics 1994;78(2):232-5.
1994: Evers-Kiebooms G; Denayer L; Welkenhuysen M; Cassiman J J; Van den Berghe H
A stigmatizing effect of the carrier status for cystic fibrosis?
Clinical genetics 1994;46(5):336-43.
1994: Dal Cin P; Sciot R; Speleman F; Samson I; Laureys G; de Potter C; Meire F; van Damme B; van den Berghe H
Chromosome aberrations in fibrous dysplasia.
Cancer genetics and cytogenetics 1994;77(2):114-7.
1994: Schoenmakers E F; Mols R; Wanschura S; Kools P F; Geurts J M; Bartnitzke S; Bullerdiek J; van den Berghe H; Van de Ven W J
Identification, molecular cloning, and characterization of the chromosome 12 breakpoint cluster region of uterine leiomyomas.
Genes, chromosomes & cancer 1994;11(2):106-18.
1994: Wlodarska I; Mecucci C; De Wolf-Peeters C; Verhoef G; Weier H U; Cassiman J J; Van Den Berghe H
"Jumping" translocation of 9q in a case of follicular lymphoma.
Cancer genetics and cytogenetics 1994;76(2):140-4.
1994: Cuneo A; Bigoni R; Balboni M; Carli M G; Piva N; Fagioli F; Latorraca A; Wlodarska I; van den Berghe H; Castoldi G
Trisomy 12 in chronic lymphocytic leukemia and hairy cell leukemia: a cytogenetic and interphase cytogenetic study.
Leukemia & lymphoma 1994;15(1-2):167-72.
1994: Dal Cin P; Sciot R; Samson I; De Smet L; De Wever I; Van Damme B; Van den Berghe H
Cytogenetic characterization of tenosynovial giant cell tumors (nodular tenosynovitis).
Cancer research 1994;54(15):3986-7.
1994: Bai X M; Van der Schueren B; Cassiman J J; Van den Berghe H; David G
Differential expression of multiple cell-surface heparan sulfate proteoglycans during embryonic tooth development.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1994;42(8):1043-54.
1994: Overbergh L; Hilliker C; Lorent K; Van Leuven F; Van den Berghe H
Identification of four genes coding for isoforms of murinoglobulin, the monomeric mouse alpha 2-macroglobulin: characterization of the exons coding for the bait region.
Genomics 1994;22(3):530-9.
1994: Umans L; Serneels L; Hilliker C; Stas L; Overbergh L; De Strooper B; Van Leuven F; Van den Berghe H
Molecular cloning of the mouse gene coding for alpha 2-macroglobulin and targeting of the gene in embryonic stem cells.
Genomics 1994;22(3):519-29.
1994: Wlodarska I; Stul M; De Wolf-Peeters C; Verhoef G; Mecucci C; Cassiman J J; Van den Berghe H
t(1;19) without detectable E2A rearrangements in two t(14;18)-positive lymphoma/leukemia cases.
Genes, chromosomes & cancer 1994;10(3):171-6.
1994: Matthijs G; Cassiman J J; Van den Berghe H; Marynen P
Characterization of the human alpha 2-macroglobulin gene promoter: identification of a novel, triple TRE/RARE/ERE response element.
Biochemical and biophysical research communications 1994;202(1):65-72.
1994: Sciot R; Dal Cin P; Brock P; Moerman P; Van Damme B; De Wever I; Casteels-Van Daele M; Van den Berghe H; Desmet V
Pleuropulmonary blastoma (pulmonary blastoma of childhood): genetic link with other embryonal malignancies?
Histopathology 1994;24(6):559-63.
1994: Smeets E; Fryns J P; Van den Berghe H
Melkersson-Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocation.
Clinical genetics 1994;45(6):323-4.
1994: Dal Cin P; Sciot R; Aly M S; Delabie J; Stas M; De Wever I; Van Damme B; Van den Berghe H
Some desmoid tumors are characterized by trisomy 8.
Genes, chromosomes & cancer 1994;10(2):131-5.
1994: Fryns J P; Hellemans M; Van den Berghe H
Macrocephaly, distinct craniofacial appearance and spastic paraplegia: an autosomal recessive subtype of complicated spastic paraplegia.
Clinical genetics 1994;45(5):228-30.
1994: Maes B; Fryns J P; Van Walleghem M; Van den Berghe H
Cognitive functioning and information processing of adult mentally retarded men with fragile-X syndrome.
American journal of medical genetics 1994;50(2):190-200.
1994: Aly M S; Dal Cin P; Van de Voorde W; van Poppel H; Ameye F; Baert L; Van den Berghe H
Chromosome abnormalities in benign prostatic hyperplasia.
Genes, chromosomes & cancer 1994;9(4):227-33.
1994: Aly M S; Dal Cin P; Jiskoot P; Deneffe G; Marynen P; Van den Berghe H
Competitive in situ hybridization in a mediastinal germ cell tumor.
Cancer genetics and cytogenetics 1994;73(1):53-6.
1994: Schoenmakers E F; Kools P F; Mols R; Kazmierczak B; Bartnitzke S; Bullerdiek J; Dal Cin P; De Jong P J; Van den Berghe H; Van de Ven W J
Physical mapping of chromosome 12q breakpoints in lipoma, pleomorphic salivary gland adenoma, uterine leiomyoma, and myxoid liposarcoma.
Genomics 1994;20(2):210-22.
1994: Aerssens J; Chaffanet M; Baens M; Matthijs G; Van den Berghe H; Cassiman J J; Marynen P
Regional assignment of seven loci to 12p13.2-pter by PCR analysis of somatic cell hybrids containing the der(12) or the der(X) chromosome from a mesothelioma showing t(X;12)(q22;p13).
Genomics 1994;20(1):119-21.
1994: Lorent K; Overbergh L; Delabie J; Van Leuven F; Van den Berghe H
Distribution of mRNA coding for alpha-2-macroglobulin, the murinoglobulins, the alpha-2-macroglobulin receptor and the alpha-2-macroglobulin receptor associated protein during mouse embryogenesis and in adult tissues.
Differentiation; research in biological diversity 1994;55(3):213-23.
1994: Fryns J P; Smeets E; Thiry P; Geutjens J; Vinken L; Van den Berghe H
Ectomorphic habitus, severe mental retardation and characteristic face: a new MCA/MR syndrome?
American journal of medical genetics 1994;49(1):91-3.
1994: Wlodarska I; De Wolf-Peeters C; Dierick H; Hilliker C; Thomas J; Mecucci C; Cassiman J J; Van den Berghe H
Detection of amplified sequences at 5q11-->q13 in a homogenously staining region found by fluorescent in situ hybridization in a case of B-cell non-Hodgkin's lymphoma.
Cytogenetics and cell genetics 1994;65(3):179-83.
1994: Hilliker C; Delabie J; Speleman F; Bilbe G; Bruggen J; Van Leuven F; Van den Berghe H
Localization of the gene (RSN) coding for restin, a marker for Reed-Sternberg cells in Hodgkin's disease, to human chromosome band 12q24.3 and YAC cloning of the locus.
Cytogenetics and cell genetics 1994;65(3):172-6.
1994: Mecucci C; van den Berghe H
Cytogenetics and immunophenotype.
Leukemia & lymphoma 1994;13 Suppl 1():49-51.
1994: Vogels A; de Smet L; van den Berghe H; Fryns J P
Thrombocytopenia and cleft hand in monosomy 21.
Genetic counseling (Geneva, Switzerland) 1994;5(1):67-71.
1994: Maes B; Fryns J P; Van Walleghem M; Van den Berghe H
Personal independence of adult mentally retarded men with fragile-X syndrome.
Genetic counseling (Geneva, Switzerland) 1994;5(2):129-39.
1994: Kleczkowska A; Decock P; van den Berghe H; Fryns J P
Borderline intelligence and discrete craniofacial dysmorphism in an adolescent female with partial trisomy 7p due to a de novo tandem duplication 7 (p15.1-->p21.3).
Genetic counseling (Geneva, Switzerland) 1994;5(4):393-7.
1994: Fryns J P; Vogels A; Haegeman J; Eggermont E; van den Berghe H
Costello syndrome: a postnatal growth retardation syndrome with distinct phenotype.
Genetic counseling (Geneva, Switzerland) 1994;5(4):337-43.
1994: Legius E; Descheemaeker M J; Fryns J P; Van den Berghe H
Neurofibromatosis type 1.
Genetic counseling (Geneva, Switzerland) 1994;5(3):225-41.
1993: Wlodarska I; Schoenmakers E; Kas K; Merregaert J; Lemahieu V; Weier U; Van den Berghe H; Van de Ven W J
Molecular mapping of the chromosome 11 breakpoint of t(11;17)(q13;q21) in a t(11;14)(q13;q32)-positive B non-Hodgkin's lymphoma.
Genes, chromosomes & cancer 1993;8(4):224-9.
1993: Sciot R; Dal Cin P; De Vos R; Van Damme B; De Wever I; Van den Berghe H; Desmet V J
Alveolar soft-part sarcoma: evidence for its myogenic origin and for the involvement of 17q25.
Histopathology 1993;23(5):439-44.
1993: David G; Bai X M; Van der Schueren B; Marynen P; Cassiman J J; Van den Berghe H
Spatial and temporal changes in the expression of fibroglycan (syndecan-2) during mouse embryonic development.
Development (Cambridge, England) 1993;119(3):841-54.
1993: Dal Cin P; Kools P; De Jonge I; Moerman P; Van de Ven W; Van den Berghe H
Rearrangement of 12q14-15 in pulmonary chondroid hamartoma.
Genes, chromosomes & cancer 1993;8(2):131-3.
1993: Derom C; Derom R; Vlietinck R; Maes H; Van den Berghe H
Iatrogenic multiple pregnancies in East Flanders, Belgium.
Fertility and sterility 1993;60(3):493-6.
1993: Fryns J P; Strømme P; van den Berghe H
Further evidence for the location of the blepharophimosis syndrome (BPES) at 3q22.3-q23.
Clinical genetics 1993;44(3):149-51.
1993: Fryns J P; Borghgraef M; Lemmens F; van den Berghe H
MCA/MR syndrome with features of Hallermann-Streiff syndrome and 4q deficiency/14q duplication.
Clinical genetics 1993;44(3):146-8.
1993: Stul M; Baens M; Mecucci C; Van den Berghe H; Cassiman J J
Rare HRAS1 alleles outside the VTR region in lymph nodes from patients with malignant lymphoma.
Cancer genetics and cytogenetics 1993;69(1):60-4.
1993: Dal Cin P; Kools P; Sciot R; De Wever I; Van Damme B; Van de Ven W; Van den Berghe H
Cytogenetic and fluorescence in situ hybridization investigation of ring chromosomes characterizing a specific pathologic subgroup of adipose tissue tumors.
Cancer genetics and cytogenetics 1993;68(2):85-90.
1993: Vanni R; Dal Cin P; Marras S; Moerman P; Andria M; Valdes E; Deprest J; Van den Berghe H
Endometrial polyp: another benign tumor characterized by 12q13-q15 changes.
Cancer genetics and cytogenetics 1993;68(1):32-3.
1993: Wlodarska I; Delabie J; De Wolf-Peeters C; Mecucci C; Stul M; Verhoef G; Cassiman J J; Van den Berghe H
T-cell lymphoma developing in Hodgkin's disease: evidence for two clones.
The Journal of pathology 1993;170(3):239-48.
1993: Busschots A M; Geerts M L; Mecucci C; Stul M; Cassiman J J; van den Berghe H
A translocation (8;14) in a cutaneous large B-cell lymphoma.
American journal of clinical pathology 1993;99(5):615-21.
1993: Fryns J P; Vogels A; Decock P; van den Berghe H
The hand-foot-genital syndrome: on the variable expression in affected males.
Clinical genetics 1993;43(5):232-4.
1993: Van Leuven F; Torrekens S; Van den Berghe H
Isolation, characterization and partial sequencing of Pregnancy Associated Mouse Protein PAMP1 identifies it as a novel female specific protein, unrelated to the alpha-2-macroglobulin family of proteinase inhibitors.
FEBS letters 1993;322(3):219-22.
1993: Devriendt K; Massa G; de Zegher F; Vanderschueren-Lodeweyckx M; Cassiman J J; Van den Berghe H; Marynen P
Opposite effects of growth hormone and estrogens on the pregnancy zone protein serum levels in children and adolescents.
Acta endocrinologica 1993;128(4):334-8.
1993: Fryns J P; Thiry P; Geutjens J; Smeets E; Vinken L; Van den Berghe H
Profound mental retardation, characteristic facies with midfacial hypoplasia and premature frontotemporal balding, muscular hypotrophy, and small patellae in two unrelated male patients.
Journal of medical genetics 1993;30(4):319-21.
1993: Baens M; Chaffanet M; Cassiman J J; van den Berghe H; Marynen P
Construction and evaluation of a hncDNA library of human 12p transcribed sequences derived from a somatic cell hybrid.
Genomics 1993;16(1):214-8.
1993: De Strooper B; Umans L; Van Leuven F; Van Den Berghe H
Study of the synthesis and secretion of normal and artificial mutants of murine amyloid precursor protein (APP): cleavage of APP occurs in a late compartment of the default secretion pathway.
The Journal of cell biology 1993;121(2):295-304.
1993: Dal Cin P; De Wolf-Peeters C; Aly M S; Deneffe G; Van Mieghem W; Van Den Berghe H
Ring chromosome 6 as the only change in a thymoma.
Genes, chromosomes & cancer 1993;6(4):243-4.
1993: Aly M S; Dal Cin P; Moerman P; De Wever I; Devriendt K; Brock P; Casteels-Van Daele M; Van den Berghe H
Loss of the Y-chromosome in a malignant Sertoli tumor.
Cancer genetics and cytogenetics 1993;65(2):104-6.
1993: Fryns J P; De Waele P; Van der Hauwaert L; Van den Berghe H
Apparent Greig cephalopolysyndactyly and sinus node disease.
American journal of medical genetics 1993;45(1):38-40.
1993: Van den Berghe H
Some genetic aspects of breast cancer.
Acta clinica Belgica. Supplementum 1993;15():17-8.
1993: Swillen A; Fryns J P; Kleczkowska A; Massa G; Vanderschueren-Lodeweyckx M; Van den Berghe H
Intelligence, behaviour and psychosocial development in Turner syndrome. A cross-sectional study of 50 pre-adolescent and adolescent girls (4-20 years).
Genetic counseling (Geneva, Switzerland) 1993;4(1):7-18.
1993: Fryns J P; Lemaire J; Timmermans J; Soekarman D; Van den Berghe H
The association of hemifacial microsomia, homolateral micro/anophthalmos, hemihypotrophy, dental anomalies, submucous cleft palate, CNS malformations and hypopigmented skin lesions following Blaschko's lines in two unrelated female patients. Further evidence for a lethal mutation surviving in mosaic form in "hypomelanosis of Ito".
Genetic counseling (Geneva, Switzerland) 1993;4(1):63-7.
1993: Fryns J P; Lenaerts J; Van den Berghe H
Larsen syndrome presenting as a familial syndrome of dwarfism, distinct oldish facial appearance and bilateral clubfeet in mother and daughter.
Genetic counseling (Geneva, Switzerland) 1993;4(1):43-6.
1993: Fryns J P; Kleczkowska A; Devriendt K; Devliegher H; Van den Berghe H
Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.
Genetic counseling (Geneva, Switzerland) 1993;4(1):37-41.
1993: Schoenmakers H F; Kools P F; Kazmierczak B; Bullerdiek J; Claussen U; Horsthemke B; Van den Berghe H; Van de Ven W J
Isolation of a somatic cell hybrid retaining the der(16)t(12;16)(q13;p11.2) from a myxoid liposarcoma cell line.
Cytogenetics and cell genetics 1993;62(2-3):159-61.
1993: Kleczkowska A; Fryns J P; Lemay P; Van den Berghe H
The characteristic phenotype of distal 9q3 trisomy is due to duplication of band 9q32.
Genetic counseling (Geneva, Switzerland) 1993;4(3):217-21.
1993: Kleczkowska A; Fryns J P; Van den Berghe H
Duplication in the long arm of the X-chromosome associated with spastic paraparesis and premature menopause.
Genetic counseling (Geneva, Switzerland) 1993;4(3):213-6.
1993: Delooz J; Van den Berghe H; Swillen A; Kleczkowska A; Fryns J P
Turner syndrome patients as adults: a study of their cognitive profile, psychosocial functioning and psychopathological findings.
Genetic counseling (Geneva, Switzerland) 1993;4(3):169-79.
1993: Kleczkowska A; Fryns J P; van den Berghe H
A distinct multiple congenital anomalies syndrome associated with distal 5q deletion (q35.1qter).
Annales de génétique 1993;36(2):126-8.
1993: Fryns J P; Kleczkowska A; Van den Berghe H
Isochromosome Xq in mosaicism with a cell line with two normal X-chromosomes: association with psychomotor retardation and neurological deficit.
Annales de génétique 1993;36(3):173-5.
1993: Kleczkowska A; Fryns J P; Decock P; Van den Berghe H
Complex chromosomal rearrangement (CCR), moderate mental retardation and discrete dysmorphic syndrome.
Genetic counseling (Geneva, Switzerland) 1993;4(4):321-4.
1993: Maes B; Fryns J P; Van Walleghem M; Van den Berghe H
Fragile-X syndrome and autism: a prevalent association or a misinterpreted connection?
Genetic counseling (Geneva, Switzerland) 1993;4(4):245-63.
1992: Fryns J P; Delooz J; van den Berghe H
Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline development.
Clinical genetics 1992;42(6):314-6.
1992: David G; Bai X M; Van der Schueren B; Cassiman J J; Van den Berghe H
Developmental changes in heparan sulfate expression: in situ detection with mAbs.
The Journal of cell biology 1992;119(4):961-75.
1992: van Leuven F; Torrekens S; Overbergh L; Lorent K; de Strooper B; van den Berghe H
The primary sequence and the subunit structure of mouse alpha-2-macroglobulin, deduced from protein sequencing of the isolated subunits and from molecular cloning of the cDNA.
European journal of biochemistry / FEBS 1992;210(1):319-27.
1992: Dal Cin P; Aly M S; De Wever I; Moerman P; Van Den Berghe H
Endometrial stromal sarcoma t(7;17)(p15-21;q12-21) is a nonrandom chromosome change.
Cancer genetics and cytogenetics 1992;63(1):43-6.
1992: Dal Cin P; Aly M S; Delabie J; Ceuppens J L; Van Gool S; Van Damme B; Baert L; Van Poppel H; Van den Berghe H
Trisomy 7 and trisomy 10 characterize subpopulations of tumor-infiltrating lymphocytes in kidney tumors and in the surrounding kidney tissue.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(20):9744-8.
1992: Mertens G; Cassiman J J; Van den Berghe H; Vermylen J; David G
Cell surface heparan sulfate proteoglycans from human vascular endothelial cells. Core protein characterization and antithrombin III binding properties.
The Journal of biological chemistry 1992;267(28):20435-43.
1992: Dal Cin P; De Wolf F; Klerckx P; Van Den Berghe H
The 6p21 chromosome region is nonrandomly involved in endometrial polyps.
Gynecologic oncology 1992;46(3):393-6.
1992: Denayer L; Evers-Kiebooms G; De Boeck K; Van den Berghe H
Reproductive decision making of aunts and uncles of a child with cystic fibrosis: genetic risk perception and attitudes toward carrier identification and prenatal diagnosis.
American journal of medical genetics 1992;44(1):104-11.
1992: Fryns J P; Delooz J; Van Den Berghe H
Unknown syndrome: nasal hypoplasia, sparse hair, truncal obesity, genital hypoplasia, and severe mental retardation.
Journal of medical genetics 1992;29(9):676-7.
1992: Dal Cin P; Van Damme B; Hoogmartens M; Van Den Berghe H
Chromosome changes in a case of hibernoma.
Genes, chromosomes & cancer 1992;5(2):178-80.
1992: Verhoef G; Van den Berghe H; Boogaerts M
Cytogenetic effects on cells derived from patients with myelodysplastic syndromes during treatment with hemopoietic growth factors.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1992;6(8):766-9.
1992: David G; van der Schueren B; Marynen P; Cassiman J J; van den Berghe H
Molecular cloning of amphiglycan, a novel integral membrane heparan sulfate proteoglycan expressed by epithelial and fibroblastic cells.
The Journal of cell biology 1992;118(4):961-9.
1992: Fryns J P; de Cock P; van den Berghe H
Occipital scalp defect associated with valvular pulmonary stenosis. A new entity?
Clinical genetics 1992;42(2):97-9.
1992: De Strooper B; Van Leuven F; Van den Berghe H
Alpha 2-macroglobulin and other proteinase inhibitors do not interfere with the secretion of amyloid precursor protein in mouse neuroblastoma cells.
FEBS letters 1992;308(1):50-3.
1992: Hilliker C; Van Leuven F; Van den Berghe H
Assignment of the gene coding for the alpha 2-macroglobulin receptor to mouse chromosome 15 and to human chromosome 12q13-q14 by isotopic and nonisotopic in situ hybridization.
Genomics 1992;13(2):472-4.
1992: Dal Cin P; Sneyers W; Aly M S; Segers A; Ostijn F; Van Damme B; Van Den Berghe H
Involvement of 19q13 in follicular thyroid adenoma.
Cancer genetics and cytogenetics 1992;60(1):99-101.
1992: Fryns J P; Schrander-Stumpel C; De Die-Smulders C; Borghgraef M; Van den Berghe H
MASA syndrome: delineation of the clinical spectrum at prepubertal age.
American journal of medical genetics 1992;43(1-2):402-7.
1992: Steyaert J; Borghgraef M; Gaulthier C; Fryns J P; Van den Berghe H
Cognitive profile in adult, normal intelligent female fragile X carriers.
American journal of medical genetics 1992;43(1-2):116-9.
1992: Verhoef G; Meeus P; Stul M; Mecucci C; Cassiman J J; Van Den Berghe H; Boogaerts M
Cytogenetic and molecular studies of the Philadelphia translocation in myelodysplastic syndromes. Report of two cases and review of the literature.
Cancer genetics and cytogenetics 1992;59(2):161-6.
1992: Decruyenaere M; Evers-Kiebooms G; Denayer L; Van den Berghe H
Cystic fibrosis: community knowledge and attitudes towards carrier screening and prenatal diagnosis.
Clinical genetics 1992;41(4):189-96.
1992: Matthijs G; Devriendt K; Cassiman J J; Van den Berghe H; Marynen P
Structure of the human alpha-2 macroglobulin gene and its promotor.
Biochemical and biophysical research communications 1992;184(2):596-603.
1992: Grubben C; de Cock P; Borghgraef M; van den Berghe H; Fryns J P
Severe pre- and postnatal growth retardation, developmental delay with hypotonia and marked hypotrophy of the distal extremities, dental anomalies, and eczematous skin. A new autosomal recessive entity.
Clinical genetics 1992;41(1):16-21.
1992: Lories V; Cassiman J J; Van den Berghe H; David G
Differential expression of cell surface heparan sulfate proteoglycans in human mammary epithelial cells and lung fibroblasts.
The Journal of biological chemistry 1992;267(2):1116-22.
1992: Kleczkowska A; Fryns J P; Lemli L; Van den Berghe H
Minimal dysmorphic stigmata in 9q deletion of paternal origin.
Genetic counseling (Geneva, Switzerland) 1992;3(1):49-52.
1992: Fryns J P; Volcke P; Van den Berghe H
The cardio-facio-cutaneous (CFC) syndrome: autosomal dominant inheritance in a large family.
Genetic counseling (Geneva, Switzerland) 1992;3(1):19-24.
1992: Soekarman D; Fryns J P; van den Berghe H
Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child.
Genetic counseling (Geneva, Switzerland) 1992;3(4):217-20.
1992: Fryns J P; Van Den Berghe H
Rieger syndrome and interstitial 4q26 deletion.
Genetic counseling (Geneva, Switzerland) 1992;3(3):153-4.
1992: Fryns J P; Dereymaeker A M; Van Den Berghe H
Hypomelanosis of Ito and severe sensorineural deafness.
Genetic counseling (Geneva, Switzerland) 1992;3(3):149-51.
1992: Hilliker C; Overbergh L; Petit P; Van Leuven F; Van den Berghe H
Assignment of mouse alpha-2-macroglobulin gene to chromosome 6 band F1-G3.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3(8):469-71.
1992: Decruyenaere M; Evers-Kiebooms G; Van den Berghe H
Community knowledge about human genetics.
Birth defects original article series 1992;28(1):167-84.
1992: Denayer L; De Boeck K; Evers-Kiebooms G; Van den Berghe H
The transfer of information about genetic transmission to brothers and sisters of parents with a CF-child.
Birth defects original article series 1992;28(1):149-58.
1992: Kleczkowska A; Fryns J P; van den Berghe H
Trisomy of the short arm of chromosome 4: the changing phenotype with age.
Annales de génétique 1992;35(4):217-23.
1991: Fryns J P; Lemmens F; van den Berghe H
Cohen syndrome: fertility in a female patient.
Clinical genetics 1991;40(6):461-4.
1991: De Strooper B; Van Leuven F; Van den Berghe H
The amyloid beta protein precursor or proteinase nexin II from mouse is closer related to its human homolog than previously reported.
Biochimica et biophysica acta 1991;1129(1):141-3.
1991: Spaepen A; Schrander-Stumpel C; Fryns J P; de Die-Smulders C; Borghgraef M; Van den Berghe H
Hallermann-Streiff syndrome: clinical and psychological findings in children. Nosologic overlap with oculodentodigital dysplasia?
American journal of medical genetics 1991;41(4):517-20.
1991: Verhoef G E; De Wolf-Peeters C; Ferrant A; Deprez S; Meeus P; Stul M; Zacheé P; Cassiman J J; Van den Berghe H; Boogaerts M A
Myelodysplastic syndromes with bone marrow fibrosis: a myelodysplastic disorder with proliferative features.
Annals of hematology 1991;63(5):235-41.
1991: Vandenberghe E; van den Oord J; Mecucci C; Van den Berghe H; De Wolf-Peeters C
B-cell non-Hodgkin's lymphomas of follicle mantle lineage: part of a biological spectrum?
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1991;5(10):829-31.
1991: Vandenberghe E; Baens M; Stul M; Bosly A; Cassiman J J; Mecucci C; Van den Berghe H
Alteration of N-ras mutation in a patient with AML M4 and trilineage myelodysplasia.
British journal of haematology 1991;79(2):338-40.
1991: Fryns J P; Bulcke J; Verdu P; Carton H; Kleczkowska A; Van den Berghe H
Apparent late-onset Cockayne syndrome and interstitial deletion of the long arm of chromosome 10 (del(10)(q11.23q21.2)).
American journal of medical genetics 1991;40(3):343-4.
1991: Walgraeve D; Verhoef G; Stul M; Cassiman J J; Mecucci C; Van den Berghe H; Boogaerts M
Chronic myelogenous leukemia after treatment with 131I for thyroid carcinoma. Report of a case and review of the literature.
Cancer genetics and cytogenetics 1991;55(2):217-24.
1991: Dal Cin P; Brock P; Aly M S; Casteels-Van Daele M; De Wever I; Van Damme B; Van den Berghe H
A variant (2;13) translocation in rhabdomyosarcoma.
Cancer genetics and cytogenetics 1991;55(2):191-5.
1991: Lukusa T; Meulepas E; Fryns J P; Van den Berghe H; Cassiman J J
"Spontaneous" FRA16B is a hot spot for sister chromatid exchanges.
Human genetics 1991;87(5):583-6.
1991: Overbergh L; Torrekens S; Van Leuven F; Van den Berghe H
Molecular characterization of the murinoglobulins.
The Journal of biological chemistry 1991;266(25):16903-10.
1991: Dal Cin P; De Wever I; Moerman P; Van den Berghe H
Translocation X;12 in mesothelioma.
Cancer genetics and cytogenetics 1991;55(1):115-8.
1991: Vandenberghe E; Martiat P; Baens M; Stul M; Ferrant A; Cuneo A; Cassiman J J; Mecucci C; Van den Berghe H
Megakaryoblastic leukemia with an N-ras mutation and late acquisition of a Philadelphia chromosome.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1991;5(8):683-6.
1991: Derom R; Vlietinck R; Derom C; Thiery M; Van Maele G; Van den Berghe H
Perinatal mortality in the East Flanders Prospective Twin Survey (preliminary results).
European journal of obstetrics, gynecology, and reproductive biology 1991;41(1):25-6.
1991: De Strooper B; Van Leuven F; Carmeliet G; Van Den Berghe H; Cassiman J J
Cultured human fibroblasts contain a large pool of precursor beta 1-integrin but lack an intracellular pool of mature subunit.
European journal of biochemistry / FEBS 1991;199(1):25-33.
1991: Stern C; Kazmierczak B; Thode B; Rommel B; Bartnitzke S; Dal Cin P; van de Ven W; Van den Berghe H; Bullerdiek J
Leiomyoma cells with 12q15 aberrations can be transformed in vitro and show a relatively stable karyotype during precrisis period.
Cancer genetics and cytogenetics 1991;54(2):223-8.
1991: Vandenberghe E; de Wolf-Peeters C; Delabie J; Thomas J; Michaux J L; Noël H; Mecucci C; Van Den Berghe H
Cytogenetic characterization of three cases of unusual B-cell non-Hodgkin's lymphoma.
Cancer genetics and cytogenetics 1991;53(2):229-35.
1991: Dal Cin P; Brock P; Casteels-Van Daele M; De Wever I; Van Damme B; Van den Berghe H
Cytogenetic characterization of congenital or infantile fibrosarcoma.
European journal of pediatrics 1991;150(8):579-81.
1991: Haspeslagh M; Fryns J P; Holvoet M; Collen G; Dierck G; Baeke J; van den Berghe H
A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation.
Clinical genetics 1991;39(6):434-41.
1991: Dal Cin P; De Wever I; Aerts R; Van Damme B; Van den Berghe H
Trisomy 8 as the only chromosome change in an epithelioid smooth muscle tumor.
Genes, chromosomes & cancer 1991;3(3):235-7.
1991: Devriendt K; Van den Berghe H; Cassiman J J; Marynen P
Primary structure of pregnancy zone protein. Molecular cloning of a full-length PZP cDNA clone by the polymerase chain reaction.
Biochimica et biophysica acta 1991;1088(1):95-103.
1991: Hillion J; Mecucci C; Aventin A; Leroux D; Wlodarska I; Van Den Berghe H; Larsen C J
A variant translocation t(2;18) in follicular lymphoma involves the 5' end of bcl-2 and Ig kappa light chain gene.
Oncogene 1991;6(1):169-72.
1991: Soekarman D; Fryns J P; Casaer P; Van Den Berghe H
Increased head circumference and facial cleft as presenting signs of the nevoid basal-cell carcinoma syndrome.
Genetic counseling (Geneva, Switzerland) 1991;2(3):157-62.
1991: Fryns J P; Van Den Berghe H
X-linked mental retardation with Marfanoid habitus: a changing phenotype with age?
Genetic counseling (Geneva, Switzerland) 1991;2(4):241-4.
1991: Fryns J P; Kleczkowska A; Kubien E; Van Den Berghe H
On the excess of mental retardation and/or congenital malformations in apparently balanced reciprocal translocations. A critical review of the Leuven data 1966-1991.
Genetic counseling (Geneva, Switzerland) 1991;2(4):185-94.
1991: Kleczkowska A; Fryns J P; Decock P; Van den Berghe H
Inverted distal duplication of the long arm of chromosome 8: borderline intelligence and discrete dysmorphic syndrome.
Genetic counseling (Geneva, Switzerland) 1991;2(2):109-13.
1991: Derom R; Vlietinck R F; Derom C; Keith L G; Van Den Berghe H
Zygosity determination at birth: a plea to the obstetrician.
Journal of perinatal medicine 1991;19 Suppl 1():234-40.
1991: Derom R; Derom C; Vlietinck R; Van Maele G; Van Den Berghe H
Twin pregnancies after medically assisted reproduction: epidemiology, comparative perinatal morbidity and mortality.
Journal of perinatal medicine 1991;19 Suppl 1():229-33.
1991: Lukusa T; Fryns J P; Kleczkowska A; Van den Berghe H
Role of gonadal dysgenesis in gonadoblastoma induction in 46, XY individuals. The Leuven experience in 46, XY pure gonadal dysgenesis and testicular feminization syndromes.
Genetic counseling (Geneva, Switzerland) 1991;2(1):9-16.
1991: Grubben C; Fryns J P; Smeets E; Van den Berghe H
Noonan phenotype in the basal cell nevus syndrome.
Genetic counseling (Geneva, Switzerland) 1991;2(1):47-54.
1991: Dal Cin P; Van den Berghe H
Isochromosome (12p) in germ cell tumors.
Recent results in cancer research. Fortschritte der Krebsforschung. Progrès dans les recherches sur le cancer 1991;123():107-11.
1991: Dereymaeker A M; Fryns J P; Ars B; Andrescescou J; Van den Berghe H
On the etiology of hearing loss in a population of 155 institutionalized children.
Acta oto-rhino-laryngologica Belgica 1991;45(3):283-91.
1990: Fryns J P; Kleczkowska A; Smeets E; Thiry P; Geutjens J; Van den Berghe H
Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).
American journal of medical genetics 1990;37(4):546-7.
1990: David G; Lories V; Decock B; Marynen P; Cassiman J J; Van den Berghe H
Molecular cloning of a phosphatidylinositol-anchored membrane heparan sulfate proteoglycan from human lung fibroblasts.
The Journal of cell biology 1990;111(6 Pt 2):3165-76.
1990: Jorissen M; Vereecke J; Carmeliet E; Van den Berghe H; Cassiman J J
Non-selective cation and dysfunctional chloride channels in the apical membrane of nasal epithelial cells cultured from cystic fibrosis patients.
Biochimica et biophysica acta 1990;1096(1):52-9.
1990: Cuppens H; Marynen P; De Boeck C; De Baets F; Eggermont E; Van den Berghe H; Cassiman J J
A child, homozygous for a stop codon in exon 11, shows milder cystic fibrosis symptoms than her heterozygous nephew.
Journal of medical genetics 1990;27(11):717-9.
1990: Lukusa T; Meulepas E; Fryns J P; Van den Berghe H; Cassiman J J
No significant increase in spontaneous and ethyl methane sulfonate-induced sister chromatid exchanges at the Xq27.3 fragile site.
Cancer genetics and cytogenetics 1990;49(1):87-94.
1990: Verhoef G E; Demuynck H; Stul M S; Cassiman J J; Mecucci C; Van Den Berghe H; Boogaerts M A
Philadelphia chromosome-positive chronic myelogenous leukemia in treated Hodgkin's disease.
Cancer genetics and cytogenetics 1990;49(2):171-6.
1990: Cuppens H; Legius E; Cabello P; Marynen P; De Boeck C; Decorte R; Fryns J P; Eggermont E; Van den Berghe H; Cassiman J J
Association between XV2c/CS7/KM19/D9 haplotypes and the delta F508 mutation. A study of 57 Belgian families.
Human genetics 1990;85(4):402-3.
1990: Vandenberghe E A; Mecucci C; Delannoy A; Van den Berghe H
Deletion of 5q by t(5;17) in therapy-related myelodysplastic syndrome.
Cancer genetics and cytogenetics 1990;48(1):49-52.
1990: Kleczkowska A; Fryns J P; Van den Berghe H
On the variable effect of mosaic normal/balanced chromosomal rearrangements in man.
Journal of medical genetics 1990;27(8):505-7.
1990: Cuneo A; Van Orshoven A; Michaux J L; Boogaerts M; Louwagie A; Doyen C; Dal Cin P; Fagioli F; Castoldi G; Van den Berghe H
Morphologic, immunologic and cytogenetic studies in erythroleukaemia: evidence for multilineage involvement and identification of two distinct cytogenetic-clinicopathological types.
British journal of haematology 1990;75(3):346-54.
1990: Kerim S; Rege-Cambrin G; Guerrasio A; Rosso C; Van Den Berghe H
Molecular cytogenetic analysis discloses complex genetic imbalance in a t(11;21) myelodysplastic syndrome.
Cancer genetics and cytogenetics 1990;46(2):243-50.
1990: Legius E; Fryns J P; Van den Berghe H
Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndrome.
Clinical genetics 1990;37(5):347-50.
1990: Borghgraef M; Fryns J P; van den Berghe H
The female and the fragile X syndrome: data on clinical and psychological findings in 7 fra(X) carriers.
Clinical genetics 1990;37(5):341-6.
1990: Heremans A; De Cock B; Cassiman J J; Van den Berghe H; David G
The core protein of the matrix-associated heparan sulfate proteoglycan binds to fibronectin.
The Journal of biological chemistry 1990;265(15):8716-24.
1990: Kerim S; Stul M; Mecucci C; Vandenberghe E; Cuneo A; Dal Cin P; Michaux J L; Louwagie A; Cassiman J J; Van den Berghe H
Rearrangement of immunoglobulin and TCR genes in lymphoid blast crisis of Ph+ chronic myeloid leukaemia.
British journal of haematology 1990;74(4):414-9.
1990: Legius E; Fryns J P; Eyskens B; Eggermont E; Desmet V; de Bethune G; Van den Berghe H
Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2)
American journal of medical genetics 1990;35(4):532-5.
1990: Zhang J; Devriendt K; Marynen P; Van den Berghe H; Cassiman J J
Chromosome mapping using polymerase chain reaction on somatic cell hybrids.
Cancer genetics and cytogenetics 1990;45(2):217-21.
1990: Fryns J P; Legius E; Dereymaeker A M; Van den Berghe H
EEC syndrome without ectrodactyly: report of two new families.
Journal of medical genetics 1990;27(3):165-8.
1990: Evers-Kiebooms G; Denayer L; Van den Berghe H
A child with cystic fibrosis: II. Subsequent family planning decisions, reproduction and use of prenatal diagnosis.
Clinical genetics 1990;37(3):207-15.
1990: Denayer L; Evers-Kiebooms G; Van den Berghe H
A child with cystic fibrosis: I. Parental knowledge about the genetic transmission of CF and about DNA-diagnostic procedures.
Clinical genetics 1990;37(3):198-206.
1990: Carmeliet G; Hauman R; Dom R; David G; Fryns J P; Van den Berghe H; Cassiman J J
Growth properties and in vitro life span of Alzheimer disease and Down syndrome fibroblasts. A blind study.
Mechanisms of ageing and development 1990;53(1):17-33.
1990: Marynen P; Devriendt K; Van den Berghe H; Cassiman J J
A genetic polymorphism in a functional domain of human pregnancy zone protein: the bait region. Genomic structure of the bait domains of human pregnancy zone protein and alpha 2 macroglobulin.
FEBS letters 1990;262(2):349-52.
1990: Fryns J P; Volcke P H; Haspeslagh M; Beusen L; Van den Berghe H
A genetic diagnostic survey in an institutionalized population of 262 moderately mentally retarded patients: the Borgerstein experience.
Journal of mental deficiency research 1990;34 ( Pt 1)():29-40.
1990: Fryns J P; Vogels A; van den Berghe H
Mental retardation, craniofacial dysmorphism, hypogonadism, diabetes mellitus and epilepsy in four siblings. A "new" mental retardation syndrome.
Clinical genetics 1990;37(2):111-6.
1990: Jorissen M; Vereecke J; Carmeliet E; Van den Berghe H; Cassiman J J
Identification of a voltage- and calcium-dependent non-selective cation channel in cultured adult and fetal human nasal epithelial cells.
Pflügers Archiv : European journal of physiology 1990;415(5):617-23.
1990: Kerim S; Mecucci C; Cuneo A; Vandenberghe E; Louwagie A; Stul M; Michaux J L; Van Den Berghe H
5q- anomaly in lymphoid disorders.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1990;4(1):12-5.
1990: Kleczkowska A; Fryns J P; Moerman P; Vandenberghe K; Van den Berghe H
Holoprosencephaly in a fetus with a 46,XX,der(7), t(7;8)(q36.1;p12) mat karyotype.
Annales de génétique 1990;33(2):111-2.
1990: Fryns J P; Vogels A; van den Berghe H
Craniosynostosis and low middle frequency perceptive deafness in mother and son. A distinct entity?
Genetic counseling (Geneva, Switzerland) 1990;1(1):63-6.
1990: Fryns J P; Kleczowska A; Decock P; van den Berghe H
Angelman's syndrome and 15q11-q13 deletion.
Genetic counseling (Geneva, Switzerland) 1990;1(1):57-62.
1990: Volcke P; Dereymaeker A M; Fryns J P; van den Berghe H
On the nosology of moderate mental retardation with special attention to X-linked mental retardation. A diagnostic genetic survey of 274 institutionalized moderately mentally retarded men.
Genetic counseling (Geneva, Switzerland) 1990;1(1):47-56.
1990: Evers-Kiebooms G; Swerts A; Van Den Berghe H
Partners of Huntington patients: implications of the disease and opinions about predictive testing and prenatal diagnosis.
Genetic counseling (Geneva, Switzerland) 1990;1(2):151-9.
1990: Kleczkowska A; Kubien E; Dmoch E; Fryns J P; Van den Berghe H
Turner syndrome: II. Associated anomalies, mental performance and psychological problems in 218 patients diagnosed in Leuven in the period 1965-1989.
Genetic counseling (Geneva, Switzerland) 1990;1(3-4):241-9.
1990: Kleczkowska A; Kubien E; Fryns J P; Van den Berghe H
Turner syndrome: the Leuven experience (1965-1989) in 478 patients. I. Patient's age at the time of diagnosis in relation to chromosomal findings.
Genetic counseling (Geneva, Switzerland) 1990;1(3-4):235-40.
1990: Kleczkowska A; Dmoch E; Kubien E; Fryns J P; Van den Berghe H
Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989.
Genetic counseling (Geneva, Switzerland) 1990;1(3-4):227-33.
1990: Fryns J P; Kleczkowska A; Van Den Berghe H
Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism.
Genetic counseling (Geneva, Switzerland) 1990;1(2):173-7.
1990: Fryns J P; Borghgraef M; Kleczkowska A; Van Den Berghe H
Ring chromosome 15: follow-up data on physical and psychological development.
Genetic counseling (Geneva, Switzerland) 1990;1(2):167-72.
1990: Fryns J P; Kleczkowska A; Van Den Berghe H
High incidence of mental retardation in Turner syndrome patients with ring chromosome X formation.
Genetic counseling (Geneva, Switzerland) 1990;1(2):161-5.
1990: Fryns J P; Volcke P; Van Den Berghe H
Martin-Bell phenotype in males with acquired central nervous system lesions. 15 males diagnosed during a systematic etiological study of 274 mentally retarded males.
Genetic counseling (Geneva, Switzerland) 1990;1(2):111-4.
1990: Grubben C; Fryns J P; De Zegher F; Van Den Berghe H
Anterior basal encephalocele in the median cleft face syndrome. Comments on nosology and treatment.
Genetic counseling (Geneva, Switzerland) 1990;1(2):103-9.
1990: Borghgraef M; Fryns J P; Van Den Berghe H
Psychological profile and behavioural characteristics in 12 patients with Prader-Willi syndrome.
Genetic counseling (Geneva, Switzerland) 1990;1(2):141-50.
1989: Heremans A; van der Schueren B; de Cock B; Paulsson M; Cassiman J J; van den Berghe H; David G
Matrix-associated heparan sulfate proteoglycan: core protein-specific monoclonal antibodies decorate the pericellular matrix of connective tissue cells and the stromal side of basement membranes.
The Journal of cell biology 1989;109(6 Pt 1):3199-211.
1989: Iurlo A; Mecucci C; Van Orshoven A; Michaux J L; Boogaerts M; Noens L; Bosly A; Louwagie A; Van Den Berghe H
Cytogenetic and clinical investigations in 76 cases with therapy-related leukemia and myelodysplastic syndrome.
Cancer genetics and cytogenetics 1989;43(2):227-41.
1989: Buttiens M; Fryns J P; van den Berghe H
An apparently new autosomal recessive syndrome with facial dysmorphism, macrocephaly, myopia and Dandy-Walker malformation.
Clinical genetics 1989;36(6):451-55.
1989: Zhang J; Marynen P; Devriendt K; Fryns J P; Van den Berghe H; Cassiman J J
Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome. Construction of a mouse-human hybrid cell line containing an i(12p) as the sole human chromosome.
Human genetics 1989;83(4):359-63.
1989: Dal Cin P; Drochmans A; Moerman P; Van den Berghe H
Isochromosome 12p in mediastinal germ cell tumor.
Cancer genetics and cytogenetics 1989;42(2):243-51.
1989: Kleczkowska A; Fryns J P; Van den Berghe H
X-to-X translocation associated with gonadal dysgenesis and discrete Turner syndrome stigmata; a case report.
European journal of obstetrics, gynecology, and reproductive biology 1989;32(3):275-9.
1989: Fryns J P; De Bisschop F; Van den Berghe H
A "new" epi-metaphyseal skeletal dysplasia in four members of a family.
Journal de génétique humaine 1989;37(3):237-41.
1989: Fryns J P; Van den Berghe H
On the occurrence of macroorchidism and mental handicap in the Aarskog syndrome.
Journal de génétique humaine 1989;37(3):221-3.
1989: Fryns J P; Moerman P; Van den Berghe H; Aymé S
[A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies. The "Fryns syndrome"]
Journal de génétique humaine 1989;37(3):203-5.
1989: Devriendt K; Zhang J; van Leuven F; van den Berghe H; Cassiman J J; Marynen P
A cluster of alpha 2-macroglobulin-related genes (alpha 2 M) on human chromosome 12p: cloning of the pregnancy-zone protein gene and an alpha 2M pseudogene.
Gene 1989;81(2):325-34.
1989: Legius E; Fryns J P; Van den Berghe H
Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome?
Journal of medical genetics 1989;26(8):522-4.
1989: Fryns J P; Chrzanowska K; Van den Berghe H
Hypohidrotic ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum.
Journal of medical genetics 1989;26(8):520-1.
1989: Kleczkowska A; Fryns J P; Standaert L; van den Berghe H
De novo Robertsonian D/D type translocations: the Leuven experience.
Clinical genetics 1989;36(1):65-8.
1989: Aventin A; Mecucci C; Van Orshoven A; Delannoy A; Van den Berghe H
Variant (3;21) translocation and megakaryocytic involvement in blastic crisis of Philadelphia positive chronic myeloid leukaemia.
British journal of haematology 1989;71(4):562-4.
1989: Kleczkowska A; Fryns J P; Steeno O; van den Berghe H
On the familial occurrence of congenital bilateral absence of vas deferens.
Clinical genetics 1989;35(4):268-71.
1989: Marynen P; Zhang J; Cassiman J J; Van den Berghe H; David G
Partial primary structure of the 48- and 90-kilodalton core proteins of cell surface-associated heparan sulfate proteoglycans of lung fibroblasts. Prediction of an integral membrane domain and evidence for multiple distinct core proteins at the cell surface of human lung fibroblasts.
The Journal of biological chemistry 1989;264(12):7017-24.
1989: Lories V; Cassiman J J; Van den Berghe H; David G
Multiple distinct membrane heparan sulfate proteoglycans in human lung fibroblasts.
The Journal of biological chemistry 1989;264(12):7009-16.
1989: David G; Lories V; Heremans A; Van der Schueren B; Cassiman J J; Van den Berghe H
Membrane-associated chondroitin sulfate proteoglycans of human lung fibroblasts.
The Journal of cell biology 1989;108(3):1165-73.
1989: De Strooper B; Van der Schueren B; Jaspers M; Saison M; Spaepen M; Van Leuven F; Van den Berghe H; Cassiman J J
Distribution of the beta 1 subgroup of the integrins in human cells and tissues.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1989;37(3):299-307.
1989: Mecucci C; Van Orshoven A; Boogaerts M; Michaux J L; Van den Berghe H
Characterization of deletions of chromosome 7 short arm occurring as primary karyotypic anomaly in acute myeloid leukaemia.
British journal of haematology 1989;71(1):13-7.
1989: Evers-Kiebooms G; Swerts A; Cassiman J J; Van den Berghe H
The motivation of at-risk individuals and their partners in deciding for or against predictive testing for Huntington's disease.
Clinical genetics 1989;35(1):29-40.
1988: Mecucci C; Delannoy A; Van den Berghe H
The origin of trisomy 12 in B-cell chronic lymphocytic leukemia.
Cancer genetics and cytogenetics 1988;36(2):203-4.
1988: Iurlo A; Mecucci C; Van Orshoven A; Michaux J L; Boogaerts M; Van den Berghe H
The karyotype in secondary hematologic disorders after treatment for Hodgkin's disease. A study of 19 patients.
Cancer genetics and cytogenetics 1988;36(2):165-72.
1988: Iurlo A; Mecucci C; Van Orshoven A; Michaux J L; Van den Berghe H
Inversion (4)(p13q28) in two cases of acute nonlymphocytic leukemia.
Cancer genetics and cytogenetics 1988;36(2):143-7.
1988: Meulepas E; Vlietinck R; van den Berghe H
The probability of dizygosity of phenotypically concordant twins.
American journal of human genetics 1988;43(6):817-26.
1988: Fryns J P; Kleczkowska A; Van den Berghe H
Familial transmission of autosomal whole arm translocation.
Journal of medical genetics 1988;25(11):783-4.
1988: Fryns J P; Kleczkowska A; Debucquoy P; van den Berghe H
Fertility and X-chromosome rearrangements: isodicentric X-chromosome formation in the mother and Xp deletion in her daughter.
Clinical genetics 1988;34(5):321-4.
1988: Fryns J P; Van den Berghe H
Is the expression of fra(2)(q13) age dependent?
Journal of medical genetics 1988;25(10):718.
1988: Lukusa T; Vercauteren P; Van den Berghe H; Cassiman J J
SCE variability in lymphocytes and fibroblasts. A controlled study.
Human genetics 1988;80(2):117-23.
1988: Fryns J P; Kleczkowska A; Smeets E; van den Berghe H
A new centromeric heteromorphism in the short arm of chromosome 20.
Journal of medical genetics 1988;25(9):636-7.
1988: Fryns J P; Dereymaeker A M; Heremans G; Marien J; van Hauwaert J; Turner G; Hockey A; van den Berghe H
Oculocerebral syndrome with hypopigmentation (Cross syndrome). Report of two siblings born to consanguineous parents.
Clinical genetics 1988;34(2):81-4.
1988: Fryns J P; Kleczkowska A; Dereymaeker A M; Van den Berghe H
Mental retardation and Y/8 translocation [karyotype: 46,XY, t(Y;8)(q12;q24)] in father and son.
Helvetica paediatrica acta 1988;43(1-2):87-90.
1988: Borghgraef M; Fryns J P; Van den Berghe H
Psychological findings in three children with ring 15 chromosome.
Journal of mental deficiency research 1988;32 ( Pt 4)():337-47.
1988: Dereymaeker A M; Fryns J P; Haegeman J; Deroover J; Van den Berghe H
A genetic-diagnostic survey in an institutionalized population of 158 mentally retarded patients. The Viaene experience.
Clinical genetics 1988;34(2):126-34.
1988: Fryns J P; Volcke P; van den Berghe H
Multiple pterygium syndrome type Escobar in two brothers. Follow-up data from childhood to adulthood.
European journal of pediatrics 1988;147(5):550-2.
1988: Van Leuven F; Marynen P; Cassiman J J; Van den Berghe H
Mapping of structure-function relationships in proteins with a panel of monoclonal antibodies. A study on human alpha 2 macroglobulin.
Journal of immunological methods 1988;111(1):39-49.
1988: Fryns J P; Moerman P; Gilis F; d'Espallier L; Van den Berghe H
Suggestively increased rate of infant death in children of fra(X) positive mothers.
American journal of medical genetics 1988;30(1-2):73-5.
1988: Fryns J P; Van den Berghe H
Inactivation pattern of the fragile X in heterozygous carriers.
American journal of medical genetics 1988;30(1-2):401-6.
1988: Fryns J P; Van den Berghe H
The concurrence of Klinefelter syndrome and fragile X syndrome.
American journal of medical genetics 1988;30(1-2):109-13.
1988: Fryns J P; Dereymaeker A M; Haegeman J; van den Berghe H
Mental retardation, macrocephaly, short stature and craniofacial dysmorphism in three sisters. A new entity among the mental retardation-macrocephaly syndromes?
Clinical genetics 1988;33(4):293-8.
1988: Mecucci C; Michaux J L; Louwagie A; Boogaerts M; Van den Berghe H
The short arm of chromosome 6 is nonrandomly rearranged in secondary myelodysplastic syndromes.
Cancer genetics and cytogenetics 1988;31(2):147-55.
1988: Jaspers M; de Strooper B; Spaepen M; van Leuven F; David G; van den Berghe H; Cassiman J J
Post-translational modification of the beta-subunit of the human fibronectin receptor.
FEBS letters 1988;231(2):402-6.
1988: Heremans A; Cassiman J J; Van den Berghe H; David G
Heparan sulfate proteoglycan from the extracellular matrix of human lung fibroblasts. Isolation, purification, and core protein characterization.
The Journal of biological chemistry 1988;263(10):4731-9.
1988: Fryns J P; Schinzel A; Van den Berghe H
Hyperlaxity in males with Melnick-Needles syndrome.
American journal of medical genetics 1988;29(3):607-11.
1988: Evers-Kiebooms G; Swerts A; van den Berghe H
Psychological aspects of amniocentesis: anxiety feelings in three different risk groups.
Clinical genetics 1988;33(3):196-206.
1988: Fryns J P; Kleczkowska A; Kubien E; van den Berghe H
[Structural chromosomal rearrangements in couples with repeated miscarriages. Experience in Louvain]
Journal de génétique humaine 1988;36(1-2):59-61.
1988: Fryns J P; Buttiens M; van den Berghe H
[Chromosome X-linked mental retardation and marfanoid syndrome]
Journal de génétique humaine 1988;36(1-2):123-8.
1988: Fryns J P; Van den Berghe H
Acrofacial dysostosis with postaxial limb deficiency.
American journal of medical genetics 1988;29(1):205-8.
1988: Fryns J P; Kleczkowska A; van den Berghe H
De novo 3q/7q translocation and associated interstitial 7q35 deletion.
Clinical genetics 1988;33(1):60-2.
1988: Fryns J P; Hofkens G; Fabry G; van den Berghe H
Isolated mesomelic shortening of the forearm in father and daughter: a new entity in the group of mesomelic dysplasias.
Clinical genetics 1988;33(1):57-9.
1988: Fryns J P; Van den Berghe H
Facial paralysis at the age of 2 months as a first clinical sign of van Buchem disease (endosteal hyperostosis).
European journal of pediatrics 1988;147(1):99-100.
1988: Mecucci C; Louwagie A; Thomas J; Boogaerts M; Van Den Berghe H
Cytogenetic studies in T-cell malignancies.
Cancer genetics and cytogenetics 1988;30(1):63-71.
1988: Mecucci C; Noens L; Aventin A; Testoni N; Van den Berghe H
Philadelphia-positive acute myelomonocytic leukemia with inversion of chromosome 16 and eosinobasophils.
American journal of hematology 1988;27(1):69-71.
1988: De Strooper B; Saison M; Jaspers M; Spaepen M; Van Leuven F; Van den Berghe H; Cassiman J J
Monoclonal antibody DH12 reacts with a cell surface and a precursor form of the beta subunit of the human fibronectin receptor.
Cell biology international reports 1988;12(1):9-16.
1988: Zhang Y; Saison M; Spaepen M; De Strooper B; Van Leuven F; David G; Van den Berghe H; Cassiman J J
Mapping of human fibronectin receptor beta subunit gene to chromosome 10.
Somatic cell and molecular genetics 1988;14(1):99-104.
1988: Van Leuven F; Marynen P; Cassiman J J; Van den Berghe H
Proteolysis of human alpha 2-macroglobulin without hydrolysis of the internal thiolesters or expression of the receptor recognition site.
The Journal of biological chemistry 1988;263(1):468-71.
1988: Vlietinck R; Derom C; Derom R; Van den Berghe H; Thiery M
The validity of Weinberg's rule in the East Flanders Prospective Twin Survey (EFPTS).
Acta geneticae medicae et gemellologiae 1988;37(2):137-41.
1988: Zhang J; Dirckx L; Marynen P; Rombauts W; Delaey B; Van den Berghe H; Cassiman J J
Mapping of rat prostatic binding protein genes C1, C2, and C3 to rat chromosome 5 by in situ hybridization.
Cytogenetics and cell genetics 1988;48(2):121-3.
1988: Evers-Kiebooms G; Denayer L; Cassiman J J; van den Berghe H
Family planning decisions after the birth of a cystic fibrosis child. The impact of prenatal diagnosis.
Scandinavian journal of gastroenterology. Supplement 1988;143():38-46.
1987: Swerts A; Evers-Kiebooms G; Van den Berghe H
Pregnancies of mothers with a neural tube defect child: outcomes and recurrence risks.
Journal de génétique humaine 1987;35(5):339-49.
1987: Fryns J P; Haspeslagh M; Dereymaeker A M; Volcke P; Van den Berghe H
A peculiar subphenotype in the fra(X) syndrome: extreme obesity-short stature-stubby hands and feet-diffuse hyperpigmentation. Further evidence of disturbed hypothalamic function in the fra(X) syndrome?
Clinical genetics 1987;32(6):388-92.
1987: de Boeck H; Lories V; David G; Cassiman J J; van den Berghe H
Identification of a 64 kDa heparan sulphate proteoglycan core protein from human lung fibroblast plasma membranes with a monoclonal antibody.
The Biochemical journal 1987;247(3):765-71.
1987: Fryns J P; Kleczkowska A; Smeets E; Van den Berghe H
Distal 11q deletion: a specific clinical entity.
Helvetica paediatrica acta 1987;42(2-3):191-4.
1987: Dereymaeker A M; Fryns J P; Hoefnagels M; Heremans G; Marien J; Van den Berghe H
The Opitz hypertelorism-hypospadias syndrome. Further delineation of the spectrum of clinical findings.
Journal de génétique humaine 1987;35(4):259-65.
1987: Mecucci C; Van Orshoven A; Vermaelen K; Michaux J L; Tricot G; Louwagie A; Delannoy A; Van den Berghe H
11q-chromosome is associated with abnormal iron stores in myelodysplastic syndromes.
Cancer genetics and cytogenetics 1987;27(1):39-44.
1987: Fryns J P; Dereymaeker A M; Hoefnagels M; D'Hondt F; Mertens G; van den Berghe H
The Brachmann-de Lange syndrome in two siblings of normal parents.
Clinical genetics 1987;31(6):413-5.
1987: Aventin A; Mecucci C; Petrick M; Noens L; van den Berghe H
Masqued Philadelphia chromosome involving the short arm of chromosome 10.
Blut 1987;54(6):371-2.
1987: Van Leuven F; Marynen P; Cassiman J J; Van den Berghe H
A mouse monoclonal antibody to human alpha 2-macroglobulin (alpha 2M) crossreacts with alpha 2M from mouse: epitope mapping and characterization of subunit structure of murine alpha 2M.
Journal of biochemistry 1987;101(5):1181-9.
1987: Rege-Cambrin G; Mecucci C; Tricot G; Michaux J L; Louwagie A; Van Hove W; Francart H; Van den Berghe H
A chromosomal profile of polycythemia vera.
Cancer genetics and cytogenetics 1987;25(2):233-45.
1987: Fryns J P; Dereymaeker A; Hoefnagels M; Van den Berghe H
Mental retardation, deafness, skeletal abnormalities, and coarse face with full lips: confirmation of the Fountain syndrome.
American journal of medical genetics 1987;26(3):551-5.
1987: Lories V; De Boeck H; David G; Cassiman J J; Van den Berghe H
Heparan sulfate proteoglycans of human lung fibroblasts. Structural heterogeneity of the core proteins of the hydrophobic cell-associated forms.
The Journal of biological chemistry 1987;262(2):854-9.
1987: Van den Berghe H; Mecucci C
Some karyotypic aspects of human leukemia.
Haematology and blood transfusion 1987;31():136-40.
1986: Fryns J P; Kleczkowska A; Dereymaeker A; Hoefnagels M; Heremans G; Marien J; van den Berghe H
A genetic-diagnostic survey in an institutionalized population of 173 severely mentally retarded patients.
Clinical genetics 1986;30(4):315-23.
1986: Mecucci C; Van Orshoven A; Tricot G; Michaux J L; Delannoy A; Van den Berghe H
Trisomy 4 identifies a subset of acute nonlymphocytic leukemias.
Blood 1986;67(5):1328-32.
1986: Dereymaeker A M; Fryns J P; Hoefnagels M; Heremans G; Marien J; van den Berghe H
The Borjeson-Forssman-Lehmann syndrome. A family study.
Clinical genetics 1986;29(4):317-20.
1986: Fryns J P; Dereymaeker A; Hoefnagels M; Volcke P; Van den Berghe H
Partial fra(X) phenotype with megalotestes in fra (X)-negative patients with acquired lesions of the central nervous system.
American journal of medical genetics 1986;23(1-2):213-9.
1986: Vercauteren P; Meulepas E; Vlietinck R; Cassiman J J; Van den Berghe H
Non-uniform distribution of sister chromatid exchanges in human lymphocytes.
Chromosoma 1986;93(3):197-202.
1986: Fryns J P; Kleczkowska A; Vinken L; Geutjens J; Smeets E; Van den Berghe H
Acrocentric/18p translocation in two mentally retarded males. Delineation of the adult phenotype.
Annales de génétique 1986;29(2):107-11.
1985: Fryns J P; Kleczkowska A; Dereymaker A M; Hoefnagels M; Heremans G; Marien J; van den Berghe H
Partial 8p trisomy due to interstitial duplication: karyotype: 46, XX, inv dup(8) (p21.1----p22).
Clinical genetics 1985;28(6):546-9.
1985: Van den Berghe H; Vermaelen K; Mecucci C; Barbieri D; Tricot G
The 5q-anomaly.
Cancer genetics and cytogenetics 1985;17(3):189-255.
1984: Haspeslagh M; Fryns J P; Beusen L; Van Dessel F; Vinken L; Moens E; Van den Berghe H
The Coffin-Lowry syndrome. A study of two new index patients and their families.
European journal of pediatrics 1984;143(2):82-6.
1984: Mecucci C; Vermaelen K; Kulling G; Michaux J L; Noens L; Van Hove W; Tricot G; Louwagie A; Van den Berghe H
Interstitial 9q- deletions in hematologic malignancies.
Cancer genetics and cytogenetics 1984;12(4):309-19.
1984: Van den Berghe H; Vermaelen K; Louwagie A; Criel A; Mecucci C; Vaerman J P
High incidence of chromosome abnormalities in IgG3 myeloma.
Cancer genetics and cytogenetics 1984;11(4):381-7.
1984: Vermaelen K; Barbieri D; Van den Berghe H
Indirect stimulation of B-cell proliferation in vitro by T cells, as evidenced by cytogenetic analysis of PHA-stimulated cell cultures of B-cell lymphomas.
Cancer genetics and cytogenetics 1984;11(4):425-8.
1984: Barbieri D; Vermaelen K; Musto P; Van den Berghe H
[Cytogenetic aspects of short-term cell cultures of lymph node, bone marrow, peripheral blood and serous effusion cells from 325 cases of Hodgkin's disease]
Recenti progressi in medicina 1984;75(3):233-40.
1984: Barbieri D; Vermaelen K; Van den Berghe H
Preliminary data on the in vitro proliferation pattern and karyotypic characteristics in cells of patients with ANLL.
Cancer genetics and cytogenetics 1984;11(1):1-9.
1984: Vercauteren P; Meulepas E; Vlietinck R; Cassiman J J; van den Berghe H
Statistical evaluation of sister chromatid exchanges.
Human genetics 1984;67(1):56-61.
1984: Vercauteren P; Meulepas E; Vlietinck R; Cassiman J J; Van den Berghe H
Statistical evaluation of sister chromatid exchanges: refined method.
Basic life sciences 1984;29 Pt A():457-67.
1983: Vermaelen K; Michaux J L; Louwagie A; Van den Berghe H
Reciprocal translocation t(6;9)(p21;q33): a new characteristic chromosome anomaly in myeloid leukemias.
Cancer genetics and cytogenetics 1983;10(2):125-31.
1983: Saison M; Verlinden J; Van Leuven F; Cassiman J J; Van den Berghe H
Identification of cell surface dipeptidylpeptidase IV in human fibroblasts.
The Biochemical journal 1983;216(1):177-83.
1983: Vermaelen K; Barbieri D; Michaux J L; Tricot G; Casteels-Van Daele M; Noens L; Van Hove W; Drochmans A; Louwagie A; Van den Berghe H
Anomalies of the long arm of chromosome 11 in human myelo- and lymphoproliferative disorders. I. Acute nonlymphocytic leukemia.
Cancer genetics and cytogenetics 1983;10(1):105-16.
1983: Mecucci C; Vermaelen K; Tricot G; Louwagie A; Michaux J L; Bosly A; Thomas J; Barbieri D; Van den Berghe H
3q-, 3q+ anomaly in malignant proliferations in humans.
Cancer genetics and cytogenetics 1983;9(4):376-81.
1983: Fryns J P; Heremans G; Marien J; Van den Berghe H
Langer-Giedion syndrome and deletion of the long arm of chromosome 8. Confirmation of the critical segment to 8q23.
Human genetics 1983;64(2):194-5.
1982: Fryns J P; Petit P; Vinken L; Geutjens J; Marien J; Van den Berghe H
Mosaic tetrasomy 21 in severe mental handicap.
European journal of pediatrics 1982;139(1):87-9.
1981: Van Leuven F; Marynen P; Cassiman J J; Van den Berghe H
Receptor-mediated endocytosis of alpha 2macroglobulin-protease complexes by fibroblasts in culture. Competitive inhibition by bacitracin.
FEBS letters 1981;134(1):83-7.
1980: Fryns J P; Bulcke J; Hens L; Van den Berghe H
Balanced transmission of centromeric fission products in man.
Human genetics 1980;54(1):127-8.
1980: Fryns J P; Vinken L; Geutjens J; Marien J; Deroover J; Van Den Berghe H
Triploid-diploid mosaïcism in a deeply mentally retarded adult.
Annales de génétique 1980;23(4):232-4.

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