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Felix Mitelman

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
189
Mandahl, Nils
164
Heim, Sverre
108
Johansson, Bertil
90
Mertens, Fredrik
64
Willén, Helena
61
Rydholm, Anders
57
Höglund, Mattias
35
Billström, Rolf
34
Fioretos, Thoas
33
Pandis, Nikos
31
Bardi, Georgia
29
Wennerberg, Johan
26
Kristoffersson, Ulf
22
Jin, Yuesheng
22
Panagopoulos, Ioannis

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Publications

TOP 3
Heim Sverre; Mitelman Felix
Molecular screening for new fusion genes in cancer.
Mitelman Felix; Johansson Bertil; Mertens Fredrik
The impact of translocations and gene fusions on cancer causation.
Mitelman Felix; Rowley Janet D
ISCN (2005) is not acceptable for describing clonal evolution in cancer.

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All Publications

2008: Heim Sverre; Mitelman Felix
Molecular screening for new fusion genes in cancer.
Nature genetics 2008;40(6):685-6.
2007: Mitelman Felix; Johansson Bertil; Mertens Fredrik
The impact of translocations and gene fusions on cancer causation.
Nature reviews. Cancer 2007;7(4):233-45.
2007: Mitelman Felix; Rowley Janet D
ISCN (2005) is not acceptable for describing clonal evolution in cancer.
Genes, chromosomes & cancer 2007;46(3):213-4.
2006: Höglund M; Frigyesi A; Mitelman F
A gene fusion network in human neoplasia.
Oncogene 2006;25(18):2674-8.
2006: Paulsson K; Békássy A N; Olofsson T; Mitelman F; Johansson B; Panagopoulos I
A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2006;20(2):224-9.
2005: Andersson Anna; Olofsson Tor; Lindgren David; Nilsson Björn; Ritz Cecilia; Edén Patrik; Lassen Carin; Råde Johan; Fontes Magnus; Mörse Helena; Heldrup Jesper; Behrendtz Mikael; Mitelman Felix; Höglund Mattias; Johansson Bertil; Fioretos Thoas
Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(52):19069-74.
2005: Höglund Mattias; Gisselsson David; Mandahl Nils; Mitelman Felix
Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours.
International journal of cancer. Journal international du cancer 2005;116(3):401-6.
2005: Mitelman Felix; Mertens Fredrik; Johansson Bertil
Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders.
Genes, chromosomes & cancer 2005;43(4):350-66.
2005: Andersson A; Edén P; Lindgren D; Nilsson J; Lassen C; Heldrup J; Fontes M; Borg A; Mitelman F; Johansson B; Höglund M; Fioretos T
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2005;19(6):1042-50.
2005: Stewénius Ylva; Gorunova Ludmila; Jonson Tord; Larsson Nina; Höglund Mattias; Mandahl Nils; Mertens Fredrik; Mitelman Felix; Gisselsson David
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(15):5541-6.
2005: Höglund Mattias; Frigyesi Attila; Säll Torbjörn; Gisselsson David; Mitelman Felix
Statistical behavior of complex cancer karyotypes.
Genes, chromosomes & cancer 2005;42(4):327-41.
2005: Paulsson Kajsa; Horvat Andrea; Fioretos Thoas; Mitelman Felix; Johansson Bertil
Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia.
Genes, chromosomes & cancer 2005;42(2):144-8.
2004: Panagopoulos Ioannis; Kitagawa Ashly; Isaksson Margareth; Mörse Helena; Mitelman Felix; Johansson Bertil
MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23).
Genes, chromosomes & cancer 2004;41(4):400-4.
2004: Nilsson Therese; Nilsson Lars; Lenhoff Stig; Rylander Lars; Astrand-Grundström Ingbritt; Strömbeck Bodil; Höglund Mattias; Turesson Ingemar; Westin Jan; Mitelman Felix; Jacobsen Sten E W; Johansson Bertil
MDS/AML-associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q).
Genes, chromosomes & cancer 2004;41(3):223-31.
2004: Höglund Mattias; Gisselsson David; Hansen Gunnar B; Mitelman Felix
Statistical dissection of cytogenetic patterns in lung cancer reveals multiple modes of karyotypic evolution independent of histological classification.
Cancer genetics and cytogenetics 2004;154(2):99-109.
2004: Zetterström Rolf; Mitelman Felix; Rydholm Anders
[Scientific fraud--the journals' dilemma]
Läkartidningen 2004;101(36):2743-4.
2004: Höglund Mattias; Gisselsson David; Soller Maria; Hansen Gunnar B; Elfving Peter; Mitelman Felix
Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.
Cancer genetics and cytogenetics 2004;153(1):1-9.
2004: Nilsson Therese; Lenhoff Stig; Rylander Lars; Höglund Mattias; Turesson Ingemar; Mitelman Felix; Westin Jan; Johansson Bertil
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparation.
British journal of haematology 2004;126(4):487-94.
2004: Bardi Georgia; Fenger Claus; Johansson Bertil; Mitelman Felix; Heim Sverre
Tumor karyotype predicts clinical outcome in colorectal cancer patients.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2004;22(13):2623-34.
2004: Storlazzi Clelia T; Fioretos Thoas; Paulsson Kajsa; Strömbeck Bodil; Lassen Carin; Ahlgren Tomas; Juliusson Gunnar; Mitelman Felix; Rocchi Mariano; Johansson Bertil
Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies.
Human molecular genetics 2004;13(14):1479-85.
2004: Frigyesi Attila; Gisselsson David; Hansen Gunnar B; Soller Maria; Mitelman Felix; Höglund Mattias
A model for karyotypic evolution in testicular germ cell tumors.
Genes, chromosomes & cancer 2004;40(3):172-8.
2004: Andersson Anna; Johansson Bertil; Lassen Carin; Mitelman Felix; Billström Rolf; Fioretos Thoas
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients.
European journal of haematology 2004;72(5):307-13.
2004: Mitelman Felix; Johansson Bertil; Mertens Fredrik
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer.
Nature genetics 2004;36(4):331-4.
2004: Höglund Mattias; Gisselsson David; Hansen Gunnar B; Mitelman Felix
Wilms tumors develop through two distinct karyotypic pathways.
Cancer genetics and cytogenetics 2004;150(1):9-15.
2004: Höglund Mattias; Jin Charlotte; Gisselsson David; Hansen Gunnar B; Mitelman Felix; Mertens Fredrik
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
Cancer genetics and cytogenetics 2004;150(1):1-8.
2004: Höglund Mattias; Sehn Laurie; Connors Joseph M; Gascoyne Randy D; Siebert Reiner; Säll Torbjörn; Mitelman Felix; Horsman Douglas E
Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas.
Genes, chromosomes & cancer 2004;39(3):195-204.
2004: Barbouti Aikaterini; Stankiewicz Pawel; Nusbaum Chad; Cuomo Christina; Cook April; Höglund Mattias; Johansson Bertil; Hagemeijer Anne; Park Sung-Sup; Mitelman Felix; Lupski James R; Fioretos Thoas
The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats.
American journal of human genetics 2004;74(1):1-10.
2004: Höglund Mattias; Gisselsson David; Hansen Gunnar B; White Valerie A; Säll Torbjörn; Mitelman Felix; Horsman Douglas
Dissecting karyotypic patterns in malignant melanomas: temporal clustering of losses and gains in melanoma karyotypic evolution.
International journal of cancer. Journal international du cancer 2004;108(1):57-65.
2004: Johansson Bertil; Mertens Fredrik; Mitelman Felix
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia.
Annals of medicine 2004;36(7):492-503.
2003: Frigyesi Attila; Gisselsson David; Mitelman Felix; Höglund Mattias
Power law distribution of chromosome aberrations in cancer.
Cancer research 2003;63(21):7094-7.
2003: Albin Maria; Björk Jonas; Welinder Hans; Tinnerberg Håkan; Mauritzson Nils; Billström Rolf; Strömberg Ulf; Mikoczy Zoli; Johansson Bertil; Ahlgren Tomas; Nilsson Per-Gunnar; Mitelman Felix; Hagmar Lars
Cytogenetic and morphologic subgroups of myelodysplastic syndromes in relation to occupational and hobby exposures.
Scandinavian journal of work, environment & health 2003;29(5):378-87.
2003: Paulsson Kajsa; Panagopoulos Ioannis; Knuutila Sakari; Jee Kowan Ja; Garwicz Stanislaw; Fioretos Thoas; Mitelman Felix; Johansson Bertil
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia.
Blood 2003;102(8):3010-5.
2003: Barbouti Aikaterini; Ahlgren Tomas; Johansson Bertil; Höglund Mattias; Lassen Carin; Turesson Ingemar; Mitelman Felix; Fioretos Thoas
Clinical and genetic studies of ETV6/ABL1-positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylate.
British journal of haematology 2003;122(1):85-93.
2003: Höglund Mattias; Gisselsson David; Hansen Gunnar B; Säll Torbjörn; Mitelman Felix
Ovarian carcinoma develops through multiple modes of chromosomal evolution.
Cancer research 2003;63(12):3378-85.
2003: Barbouti Aikaterini; Höglund Mattias; Johansson Bertil; Lassen Carin; Nilsson Per-Gunnar; Hagemeijer Anne; Mitelman Felix; Fioretos Thoas
A novel gene, MSI2, encoding a putative RNA-binding protein is recurrently rearranged at disease progression of chronic myeloid leukemia and forms a fusion gene with HOXA9 as a result of the cryptic t(7;17)(p15;q23).
Cancer research 2003;63(6):1202-6.
2003: Nilsson Thérèse; Höglund Mattias; Lenhoff Stig; Rylander Lars; Turesson Ingemar; Westin Jan; Mitelman Felix; Johansson Bertil
A pooled analysis of karyotypic patterns, breakpoints and imbalances in 783 cytogenetically abnormal multiple myelomas reveals frequently involved chromosome segments as well as significant age- and sex-related differences.
British journal of haematology 2003;120(6):960-9.
2003: Panagopoulos Ioannis; Isaksson Margareth; Billström Rolf; Strömbeck Bodil; Mitelman Felix; Johansson Bertil
Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13).
Genes, chromosomes & cancer 2003;36(1):107-12.
2003: Panagopoulos Ioannis; Isaksson Margareth; Lindvall Charlotta; Hagemeijer Anna; Mitelman Felix; Johansson Bertil
Genomic characterization of MOZ/CBP and CBP/MOZ chimeras in acute myeloid leukemia suggests the involvement of a damage-repair mechanism in the origin of the t(8;16)(p11;p13).
Genes, chromosomes & cancer 2003;36(1):90-8.
2002: Mauritzson N; Albin M; Rylander L; Billström R; Ahlgren T; Mikoczy Z; Björk J; Strömberg U; Nilsson P G; Mitelman F; Hagmar L; Johansson B
Pooled analysis of clinical and cytogenetic features in treatment-related and de novo adult acute myeloid leukemia and myelodysplastic syndromes based on a consecutive series of 761 patients analyzed 1976-1993 and on 5098 unselected cases reported in the literature 1974-2001.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2002;16(12):2366-78.
2002: Panagopoulos Ioannis; Fioretos Thoas; Isaksson Margareth; Mitelman Felix; Johansson Bertil; Theorin Niklas; Juliusson Gunnar
RT-PCR analysis of acute myeloid leukemia with t(8;16)(p11;p13): identification of a novel MOZ/CBP transcript and absence of CBP/MOZ expression.
Genes, chromosomes & cancer 2002;35(4):372-4.
2002: Höglund Mattias; Gisselsson David; Hansen Gunnar B; Säll Torbjörn; Mitelman Felix; Nilbert Mef
Dissecting karyotypic patterns in colorectal tumors: two distinct but overlapping pathways in the adenoma-carcinoma transition.
Cancer research 2002;62(20):5939-46.
2002: Barbouti Aikaterini; Johansson Bertil; Höglund Mattias; Mauritzson Nils; Strömbeck Bodil; Nilsson Per-Gunnar; Tanke Hans J; Hagemeijer Anne; Mitelman Felix; Fioretos Thoas
Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.
Genes, chromosomes & cancer 2002;35(2):127-37.
2002: Billström R; Ahlgren T; Békássy A N; Malm C; Olofsson T; Höglund M; Mitelman F; Johansson B
Acute myeloid leukemia with inv(16)(p13q22): involvement of cervical lymph nodes and tonsils is common and may be a negative prognostic sign.
American journal of hematology 2002;71(1):15-9.
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: Nilsson T; Lenhoff S; Turesson I; Rylander L; Mitelman F; Westin J; Höglund M; Johansson B
Cytogenetic features of multiple myeloma: impact of gender, age, disease phase, culture time, and cytokine stimulation.
European journal of haematology 2002;68(6):345-53.
2002: Höglund Mattias; Gisselsson David; Säll Torbjörn; Mitelman Felix
Coping with complexity. multivariate analysis of tumor karyotypes.
Cancer genetics and cytogenetics 2002;135(2):103-9.
2002: Panagopoulos Ioannis; Fioretos Thoas; Isaksson Margareth; Larsson Gun; Billström Rolf; Mitelman Felix; Johansson Bertil
Expression of NUP98/TOP1, but not of TOP1/NUP98, in a treatment-related myelodysplastic syndrome with t(10;20;11)(q24;q11;p15).
Genes, chromosomes & cancer 2002;34(2):249-54.
2002: Höglund Mattias; Gisselsson David; Hansen Gunnar B; Säll Torbjörn; Mitelman Felix
Multivariate analysis of chromosomal imbalances in breast cancer delineates cytogenetic pathways and reveals complex relationships among imbalances.
Cancer research 2002;62(9):2675-80.
2002: Olney Harold J; Mitelman Felix; Johansson Bertil; Mrózek Krzysztof; Berger Roland; Rowley Janet D
Unique balanced chromosome abnormalities in treatment-related myelodysplastic syndromes and acute myeloid leukemia: report from an international workshop.
Genes, chromosomes & cancer 2002;33(4):413-23.
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.
2002: Jerkeman M; Aman P; Cavallin-Stahl E; Torlakovic E; Akerman M; Mitelman F; Fioretos T
Prognostic implications of BCL6 rearrangement in uniformly treated patients with diffuse large B-cell lymphoma--a Nordic Lymphoma Group study.
International journal of oncology 2002;20(1):161-5.
2002: Johansson Bertil; Fioretos Thoas; Mitelman Felix
Cytogenetic and molecular genetic evolution of chronic myeloid leukemia.
Acta haematologica 2002;107(2):76-94.
2001: Fioretos T; Panagopoulos I; Lassen C; Swedin A; Billström R; Isaksson M; Strömbeck B; Olofsson T; Mitelman F; Johansson B
Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL.
Genes, chromosomes & cancer 2001;32(4):302-10.
2001: Höglund M; Säll T; Heim S; Mitelman F; Mandahl N; Fadl-Elmula I
Identification of cytogenetic subgroups and karyotypic pathways in transitional cell carcinoma.
Cancer research 2001;61(22):8241-6.
2001: Björk J; Albin M; Welinder H; Tinnerberg H; Mauritzson N; Kauppinen T; Strömberg U; Johansson B; Billström R; Mikoczy Z; Ahlgren T; Nilsson P G; Mitelman F; Hagmar L
Are occupational, hobby, or lifestyle exposures associated with Philadelphia chromosome positive chronic myeloid leukaemia?
Occupational and environmental medicine 2001;58(11):722-7.
2001: Gisselsson D; Jonson T; Petersén A; Strömbeck B; Dal Cin P; Höglund M; Mitelman F; Mertens F; Mandahl N
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(22):12683-8.
2001: Paulsson K; Säll T; Fioretos T; Mitelman F; Johansson B
The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology.
Cancer genetics and cytogenetics 2001;130(2):160-5.
2001: Andersson A; Höglund M; Johansson B; Lassen C; Billström R; Garwicz S; Nilsson P G; Mitelman F; Fioretos T
Paired multiplex reverse-transcriptase polymerase chain reaction (PMRT-PCR) analysis as a rapid and accurate diagnostic tool for the detection of MLL fusion genes in hematologic malignancies.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2001;15(8):1293-300.
2001: Höglund M; Gisselsson D; Mandahl N; Johansson B; Mertens F; Mitelman F; Säll T
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution.
Genes, chromosomes & cancer 2001;31(2):156-71.
2001: Mauritzson N; Johansson B; Rylander L; Albin M; Strömberg U; Billström R; Ahlgren T; Mikoczy Z; Mitelman F; Hagmar L; Nilsson P G
The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex.
British journal of haematology 2001;113(2):347-56.
2001: Johansson B; Axelsson P; Billström R; Strömbeck B; Arheden K; Olofsson T; Cervin A; Adriansson M; Tanke H J; Mitelman F; Fioretos T
Isodicentric 7p, idic(7)(q11.2), in acute myeloid leukemia associated with older age and favorable response to induction chemotherapy: a new clinical entity?
Genes, chromosomes & cancer 2001;30(3):261-6.
2001: Panagopoulos I; Fioretos T; Isaksson M; Samuelsson U; Billström R; Strömbeck B; Mitelman F; Johansson B
Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13).
Human molecular genetics 2001;10(4):395-404.
2001: Jin C; Martins C; Jin Y; Wiegant J; Wennerberg J; Dictor M; Gisselsson D; Strömbeck B; Fonseca I; Mitelman F; Tanke H J; Höglund M; Mertens F
Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH.
Genes, chromosomes & cancer 2001;30(2):161-7.
2000: Albin M; Björk J; Welinder H; Tinnerberg H; Mauritzson N; Johansson B; Billström R; Strömberg U; Mikoczy Z; Ahlgren T; Nilsson P G; Mitelman F; Hagmar L
Acute myeloid leukemia and clonal chromosome aberrations in relation to past exposure to organic solvents.
Scandinavian journal of work, environment & health 2000;26(6):482-91.
2000: Panagopoulos I; Teixeira M R; Micci F; Hammerstrøm J; Isaksson M; Johansson B; Mitelman F; Heim S
Acute myeloid leukemia with inv(8)(p11q13).
Leukemia & lymphoma 2000;39(5-6):651-6.
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: Fadl-Elmula I; Gorunova L; Mandahl N; Elfving P; Lundgren R; Mitelman F; Heim S
Karyotypic characterization of urinary bladder transitional cell carcinomas.
Genes, chromosomes & cancer 2000;29(3):256-65.
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: Panagopoulos I; Isaksson M; Lindvall C; Björkholm M; Ahlgren T; Fioretos T; Heim S; Mitelman F; Johansson B
RT-PCR analysis of the MOZ-CBP and CBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13).
Genes, chromosomes & cancer 2000;28(4):415-24.
2000: Andreasson P; Höglund M; Békássy A N; Garwicz S; Heldrup J; Mitelman F; Johansson B
Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias.
European journal of haematology 2000;65(1):40-51.
2000: Mauritzson N; Johansson B; Albin M; Rylander L; Billström R; Ahlgren T; Mikoczy Z; Strömberg U; Mitelman F; Hagmar L; Nilsson P G
Survival time in a population-based consecutive series of adult acute myeloid leukemia--the prognostic impact of karyotype during the time period 1976-1993.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2000;14(6):1039-43.
2000: Gisselsson D; Pettersson L; Höglund M; Heidenblad M; Gorunova L; Wiegant J; Mertens F; Dal Cin P; Mitelman F; Mandahl N
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(10):5357-62.
2000: Mitelman F
Recurrent chromosome aberrations in cancer.
Mutation research 2000;462(2-3):247-53.
2000: Johansson B; Fioretos T; Kullendorff C M; Wiebe T; Békássy A N; Garwicz S; Forestier E; Roos G; Akerman M; Mitelman F; Billström R
Granulocytic sarcomas in body cavities in childhood acute myeloid leukemias with 11q23/MLL rearrangements.
Genes, chromosomes & cancer 2000;27(2):136-42.
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: Mertens F; Larramendy M; Gustavsson A; Gisselsson D; Rydholm A; Brosjö O; Mitelman F; Knuutila S; Mandahl N
Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p.
Cancer genetics and cytogenetics 2000;116(2):89-96.
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.
1999: Fadl-Elmula I; Gorunova L; Mandahl N; Elfving P; Lundgren R; Mitelman F; Heim S
Cytogenetic monoclonality in multifocal uroepithelial carcinomas: evidence of intraluminal tumour seeding.
British journal of cancer 1999;81(1):6-12.
1999: Adeyinka A; Mertens F; Idvall I; Bondeson L; Ingvar C; Mitelman F; Pandis N
Different patterns of chromosomal imbalances in metastasising and non-metastasising primary breast carcinomas.
International journal of cancer. Journal international du cancer 1999;84(4):370-5.
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: 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: Johansson B; Billström R; Broberg K; Fioretos T; Nilsson P G; Ahlgren T; Malm C; Samuelsson B O; Mitelman F
Cytogenetic polyclonality in hematologic malignancies.
Genes, chromosomes & cancer 1999;24(3):222-9.
1999: Jerkeman M; Johansson B; Akerman M; Cavallin-Ståhl E; Kristoffersson U; Mitelman F
Prognostic implications of cytogenetic aberrations in diffuse large B-cell lymphomas.
European journal of haematology 1999;62(3):184-90.
1999: Mauritzson N; Johansson B; Albin M; Billström R; Ahlgren T; Mikoczy Z; Nilsson P G; Hagmar L; Mitelman F
A single-center population-based consecutive series of 1500 cytogenetically investigated adult hematological malignancies: karyotypic features in relation to morphology, age and gender.
European journal of haematology 1999;62(2):95-102.
1998: Gisselsson D; Höglund M; Mertens F; Mitelman F; Mandahl N
Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization.
Genes, chromosomes & cancer 1998;23(3):203-12.
1998: Gorunova L; Höglund M; Andrén-Sandberg A; Dawiskiba S; Jin Y; Mitelman F; Johansson B
Cytogenetic analysis of pancreatic carcinomas: intratumor heterogeneity and nonrandom pattern of chromosome aberrations.
Genes, chromosomes & cancer 1998;23(2):81-99.
1998: Hagmar L; Bonassi S; Strömberg U; Mikoczy Z; Lando C; Hansteen I L; Montagud A H; Knudsen L; Norppa H; Reuterwall C; Tinnerberg H; Brogger A; Forni A; Högstedt B; Lambert B; Mitelman F; Nordenson I; Salomaa S; Skerfving S
Cancer predictive value of cytogenetic markers used in occupational health surveillance programs: a report from an ongoing study by the European Study Group on Cytogenetic Biomarkers and Health.
Mutation research 1998;405(2):171-8.
1998: Andreasson P; Höglund M; Jonson T; Békàssy A; Mitelman F; Johansson B
Molecular characterization of jumping translocations reveals spatial and temporal breakpoint heterogeneity.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1998;12(9):1411-6.
1998: Parada L A; Hallén M; Tranberg K G; Hägerstrand I; Bondeson L; Mitelman F; Johansson B
Frequent rearrangements of chromosomes 1, 7, and 8 in primary liver cancer.
Genes, chromosomes & cancer 1998;23(1):26-35.
1998: Jin C; Jin Y; Höglund M; Wennerberg J; Akervall J; Willén R; Dictor M; Mandahl N; Mitelman F; Mertens F
Cytogenetic and molecular genetic demonstration of polyclonality in an acinic cell carcinoma.
British journal of cancer 1998;78(3):292-5.
1998: Adeyinka A; Mertens F; Idvall I; Bondeson L; Ingvar C; Heim S; Mitelman F; Pandis N
Cytogenetic findings in invasive breast carcinomas with prognostically favourable histology: a less complex karyotypic pattern?
International journal of cancer. Journal international du cancer 1998;79(4):361-4.
1998: Jin Y; Höglund M; Jin C; Martins C; Wennerberg J; Akervall J; Mandahl N; Mitelman F; Mertens F
FISH characterization of head and neck carcinomas reveals that amplification of band 11q13 is associated with deletion of distal 11q.
Genes, chromosomes & cancer 1998;22(4):312-20.
1998: Nilsson T; Andreasson P; Höglund M; Fioretos T; Billström R; Garwicz S; Mitelman F; Johansson B
ETV6/ABL fusion is rare in Ph-negative chronic myeloid disorders.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1998;12(7):1167-8.
1998: Pandis N; Teixeira M R; Adeyinka A; Rizou H; Bardi G; Mertens F; Andersen J A; Bondeson L; Sfikas K; Qvist H; Apostolikas N; Mitelman F; Heim S
Cytogenetic comparison of primary tumors and lymph node metastases in breast cancer patients.
Genes, chromosomes & cancer 1998;22(2):122-9.
1998: Mandahl N; Mertens F; Willén H; Rydholm A; Kreicbergs A; Mitelman F
Nonrandom pattern of telomeric associations in atypical lipomatous tumors with ring and giant marker chromosomes.
Cancer genetics and cytogenetics 1998;103(1):25-34.
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: Fadl-Elmula I; Gorunova L; Lundgren R; Mandahl N; Forsby N; Mitelman F; Heim S
Chromosomal abnormalities in two bladder carcinomas with secondary squamous cell differentiation.
Cancer genetics and cytogenetics 1998;102(2):125-30.
1998: Andreasson P; Johansson B; Arheden K; Kristoffersson U; Akerman M; Mitelman F; Höglund M
Genomic amplification of CCND2 is rare in non-Hodgkin lymphomas.
Cancer genetics and cytogenetics 1998;102(1):81-2.
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: Andreasson P; Johansson B; Billström R; Garwicz S; Mitelman F; Höglund M
Fluorescence in situ hybridization analyses of hematologic malignancies reveal frequent cytogenetically unrecognized 12p rearrangements.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1998;12(3):390-400.
1998: Mencinger M; Panagopoulos I; Contreras J A; Mitelman F; Aman P
Expression analysis and chromosomal mapping of a novel human gene, APRIL, encoding an acidic protein rich in leucines.
Biochimica et biophysica acta 1998;1395(2):176-80.
1998: Höglund M; Gorunova L; Andrén-Sandberg A; Dawiskiba S; Mitelman F; Johansson B
Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: frequent loss of 19p13.3 and gain of 19q13.1-13.2.
Genes, chromosomes & cancer 1998;21(1):8-16.
1998: Schuborg C; Mertens F; Rydholm A; Brosjö O; Dictor M; Mitelman F; Mandahl N
Cytogenetic analysis of four angiosarcomas from deep and superficial soft tissue.
Cancer genetics and cytogenetics 1998;100(1):52-6.
1998: Hagmar L; Bonassi S; Strömberg U; Mikoczy Z; Lando C; Hansteen I L; Montagud A H; Knudsen L; Norppa H; Reuterwall C; Tinnerberg H; Brøgger A; Forni A; Högstedt B; Lambert B; Mitelman F; Nordenson I; Salomaa S; Skerfving S
Cancer predictive value of cytogenetic markers used in occupational health surveillance programs.
Recent results in cancer research. Fortschritte der Krebsforschung. Progrès dans les recherches sur le cancer 1998;154():177-84.
1997: Johansson B; Brøndum-Nielsen K; Billström R; Schiødt I; Mitelman F
Translocations between the long arms of chromosomes 1 and 5 in hematologic malignancies are strongly associated with neoplasms of the myeloid lineages.
Cancer genetics and cytogenetics 1997;99(2):97-101.
1997: Elfving P; Mandahl N; Lundgren R; Limon J; Bak-Jensen E; Fernö M; Olsson H; Mitelman F
Prognostic implications of cytogenetic findings in kidney cancer.
British journal of urology 1997;80(5):698-706.
1997: Andreasson P; Johansson B; Carlsson M; Jarlsfelt I; Fioretos T; Mitelman F; Höglund M
BCR/ABL-negative chronic myeloid leukemia with ETV6/ABL fusion.
Genes, chromosomes & cancer 1997;20(3):299-304.
1997: Parada L A; Bardi G; Hallén M; Hägerstrand I; Tranberg K G; Mitelman F; Johansson B
Cytogenetic abnormalities and clonal evolution in an adult hepatoblastoma.
The American journal of surgical pathology 1997;21(11):1381-6.
1997: Panagopoulos I; Lassen C; Isaksson M; Mitelman F; Mandahl N; Aman P
Characteristic sequence motifs at the breakpoints of the hybrid genes FUS/CHOP, EWS/CHOP and FUS/ERG in myxoid liposarcoma and acute myeloid leukemia.
Oncogene 1997;15(11):1357-62.
1997: Adeyinka A; Pandis N; Bardi G; Bonaldi L; Mertens F; Mitelman F; Heim S
A subgroup of breast carcinomas is cytogenetically characterized by trisomy 12.
Cancer genetics and cytogenetics 1997;97(2):119-21.
1997: Johansson B; Billström R; Kristoffersson U; Akerman M; Garwicz S; Ahlgren T; Malm C; Mitelman F
Deletion of chromosome arm 3p in hematologic malignancies.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(8):1207-13.
1997: Bardi G; Parada L A; Bomme L; Pandis N; Johansson B; Willén R; Fenger C; Kronborg O; Mitelman F; Heim S
Cytogenetic findings in metastases from colorectal cancer.
International journal of cancer. Journal international du cancer 1997;72(4):604-7.
1997: Panagopoulos I; Thelin S; Mertens F; Mitelman F; Aman P
Variable FHIT transcripts in non-neoplastic tissues.
Genes, chromosomes & cancer 1997;19(4):215-9.
1997: Billström R; Johansson B; Fioretos T; Garwicz S; Malm C; Zettervall O; Mitelman F
Poor survival in t(8;21) (q22;q22)-associated acute myeloid leukaemia with leukocytosis.
European journal of haematology 1997;59(1):47-52.
1997: Andreasson P; Johansson B; Strömbeck B; Donnér M; Mitelman F; Höglund M
Childhood acute lymphoblastic leukaemia with ider(21)(q10)t(12;21)(p12;q22): a new recurrent abnormality showing ETV6/CBFA2 fusion.
British journal of haematology 1997;98(1):216-8.
1997: Mertens F; Johansson B; Höglund M; Mitelman F
Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms.
Cancer research 1997;57(13):2765-80.
1997: Andreasson P; Johansson B; Arheden K; Billström R; Mitelman F; Höglund M
Deletions of CDKN1B and ETV6 in acute myeloid leukemia and myelodysplastic syndromes without cytogenetic evidence of 12p abnormalities.
Genes, chromosomes & cancer 1997;19(2):77-83.
1997: Mencinger M; Panagopoulos I; Andreasson P; Lassen C; Mitelman F; Aman P
Characterization and chromosomal mapping of the human TFG gene involved in thyroid carcinoma.
Genomics 1997;41(3):327-31.
1997: Mitelman F; Johansson B; Mandahl N; Mertens F
Clinical significance of cytogenetic findings in solid tumors.
Cancer genetics and cytogenetics 1997;95(1):1-8.
1997: Mitelman F; Mertens F; Johansson B
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia.
Nature genetics 1997;15 Spec No():417-74.
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: Pandis N; Bardi G; Mitelman F; Heim S
Deletion of the short arm of chromosome 3 in breast tumors.
Genes, chromosomes & cancer 1997;18(4):241-5.
1997: Jin C; Jin Y; Wennerberg J; Akervall J; Dictor M; Mandahl N; Heim S; Mitelman F; Mertens F
Cytogenetic analysis of inverted nasal papillomas and demonstration of genetic convergence during in vitro passaging.
International journal of cancer. Journal international du cancer 1997;70(6):668-73.
1997: Jin C; Jin Y; Wennerberg J; Akervall J; Grenthe B; Mandahl N; Heim S; Mitelman F; Mertens F
Clonal chromosome aberrations accumulate with age in upper aerodigestive tract mucosa.
Mutation research 1997;374(1):63-72.
1997: Parada L A; Bardi G; Hallén M; Hägerstrand I; Tranberg K G; Mitelman F; Johansson B
Monosomy 22 in a case of biliary adenofibroma.
Cancer genetics and cytogenetics 1997;93(2):183-4.
1997: Petersson C; Pandis N; Rizou H; Mertens F; Dietrich C U; Adeyinka A; Idvall I; Bondeson L; Georgiou G; Ingvar C; Heim S; Mitelman F
Karyotypic abnormalities in fibroadenomas of the breast.
International journal of cancer. Journal international du cancer 1997;70(3):282-6.
1997: Billström R; Johansson B; Strömbeck B; el-Rifai W; Larramendy M; Olofsson T; Mitelman F; Knuutila S
Clonal CD5-positive B lymphocytes in myelodysplastic syndrome with systemic vasculitis and trisomy 8.
Annals of hematology 1997;74(1):37-40.
1997: Bardi G; Parada L A; Bomme L; Pandis N; Willén R; Johansson B; Jeppsson B; Beroukas K; Heim S; Mitelman F
Cytogenetic comparisons of synchronous carcinomas and polyps in patients with colorectal cancer.
British journal of cancer 1997;76(6):765-9.
1996: Pejovic T; Iosif C S; Mitelman F; Heim S
Karyotypic characteristics of borderline malignant tumors of the ovary: trisomy 12, trisomy 7, and r(1) as nonrandom features.
Cancer genetics and cytogenetics 1996;92(2):95-8.
1996: Mertens F; Pålsson E; Lindstrand A; Toksvig-Larsen S; Knuutila S; Larramendy M L; el-Rifai W; Limon J; Mitelman F; Mandahl N
Evidence of somatic mutations in osteoarthritis.
Human genetics 1996;98(6):651-6.
1996: Mertens F; Johansson B; Mitelman F
Dichotomy of hyperdiploid acute lymphoblastic leukemia on the basis of the distribution of gained chromosomes.
Cancer genetics and cytogenetics 1996;92(1):8-10.
1996: Panagopoulos I; Pandis N; Thelin S; Petersson C; Mertens F; Borg A; Kristoffersson U; Mitelman F; Aman P
The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14.
Cancer research 1996;56(21):4871-5.
1996: Aman P; Panagopoulos I; Lassen C; Fioretos T; Mencinger M; Toresson H; Höglund M; Forster A; Rabbitts T H; Ron D; Mandahl N; Mitelman F
Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS.
Genomics 1996;37(1):1-8.
1996: Panagopoulos I; Aman P; Mertens F; Mandahl N; Rydholm A; Bauer H F; Mitelman F
Genomic PCR detects tumor cells in peripheral blood from patients with myxoid liposarcoma.
Genes, chromosomes & cancer 1996;17(2):102-7.
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: 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: Petersson C; Pandis N; Mertens F; Adeyinka A; Ingvar C; Ringberg A; Idvall I; Bondeson L; Borg A; Olsson H; Kristoffersson U; Mitelman F
Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families.
Genes, chromosomes & cancer 1996;16(3):185-8.
1996: Johansson B; Mertens F; Mitelman F
Primary vs. secondary neoplasia-associated chromosomal abnormalities--balanced rearrangements vs. genomic imbalances?
Genes, chromosomes & cancer 1996;16(3):155-63.
1996: Akerman M; Dreinhöfer K; Rydholm A; Willén H; Mertens F; Mitelman F; Mandahl N
Cytogenetic studies on fine-needle aspiration samples from osteosarcoma and Ewing's sarcoma.
Diagnostic cytopathology 1996;15(1):17-22.
1996: Mertens F; Jonsson K; Willén H; Rydholm A; Kreicbergs A; Eriksson L; Olsson-Sandin G; Mitelman F; Mandahl N
Chromosome rearrangements in synovial chondromatous lesions.
British journal of cancer 1996;74(2):251-4.
1996: Johansson B; Fioretos T; Billström R; Mitelman F
Abberant cytogenetic evolution pattern of Philadelphia-positive chronic myeloid leukemia treated with interferon-alpha.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(7):1134-8.
1996: Choong P F; Mandahl N; Mertens F; Willén H; Alvegård T; Kreicbergs A; Mitelman F; Rydholm A
19p+ marker chromosome correlates with relapse in malignant fibrous histiocytoma.
Genes, chromosomes & cancer 1996;16(2):88-93.
1996: Köhler M; Johansson B; Garwicz S; Heim S; Mitelman F
No FISH evidence for trisomy 7 in normal or leukemic bone marrow.
Cancer genetics and cytogenetics 1996;88(2):133-5.
1996: Adeyinka A; Pandis N; Nilsson J; Idvall I; Mertens F; Petersson C; Heim S; Mitelman F
Different cytogenetic patterns in skeletal breast cancer metastases.
Genes, chromosomes & cancer 1996;16(1):72-4.
1996: Pejovic T; Alm P; Iosif S C; Mitelman F; Heim S
Cytogenetic findings in four malignant mixed mesodermal tumors of the ovary.
Cancer genetics and cytogenetics 1996;88(1):53-6.
1996: Pandis N; Idvall I; Bardi G; Jin Y; Gorunova L; Mertens F; Olsson H; Ingvar C; Beroukas K; Mitelman F; Heim S
Correlation between karyotypic pattern and clincopathologic features in 125 breast cancer cases.
International journal of cancer. Journal international du cancer 1996;66(2):191-6.
1996: Jin Y; Mertens F; Jin C; Wennerberg J; Mandahl N; Heim S; Mitelman F
Clonal chromosome abnormalities in two chemodectomas.
Genes, chromosomes & cancer 1996;15(3):178-81.
1996: Panagopoulos I; Höglund M; Mertens F; Mandahl N; Mitelman F; Aman P
Fusion of the EWS and CHOP genes in myxoid liposarcoma.
Oncogene 1996;12(3):489-94.
1996: Johansson B; Fioretos T; Garwicz S; Heim S; Mitelman F
t(3;21)(q26;q22) with AML1 rearrangement in a de novo childhood acute monoblastic leukaemia.
British journal of haematology 1996;92(2):429-31.
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: Panagopoulos I; Aman P; Johansson B; Malm C; Lenhoff S; Billström R; Mitelman F
NRAS mutations are rare in acute myeloid leukaemias with t(8;21) or inv(16).
European journal of haematology 1996;56(1-2):68-71.
1996: Höglund M; Johansson B; Pedersen-Bjergaard J; Marynen P; Mitelman F
Molecular characterization of 12p abnormalities in hematologic malignancies: deletion of KIP1, rearrangement of TEL, and amplification of CCND2.
Blood 1996;87(1):324-30.
1996: Teixeira M R; Pandis N; Gerdes A M; Dietrich C U; Bardi G; Andersen J A; Graversen H P; Mitelman F; Heim S
Cytogenetic abnormalities in an in situ ductal carcinoma and five prophylactically removed breasts from members of a family with hereditary breast cancer.
Breast cancer research and treatment 1996;38(2):177-82.
1995: Gorunova L; Johansson B; Dawiskiba S; Andrén-Sandberg A; Jin Y; Mandahl N; Heim S; Mitelman F
Massive cytogenetic heterogeneity in a pancreatic carcinoma: fifty-four karyotypically unrelated clones.
Genes, chromosomes & cancer 1995;14(4):259-66.
1995: Mertens F; Willén H; Rydholm A; Brosjö O; Carlén B; Mitelman F; Mandahl N
Trisomy 20 is a primary chromosome aberration in desmoid tumors.
International journal of cancer. Journal international du cancer 1995;63(4):527-9.
1995: Johansson B; Mertens F; Mitelman F
Cytogenetic evolution patterns in non-Hodgkin's lymphoma.
Blood 1995;86(10):3905-14.
1995: Akervall J A; Jin Y; Wennerberg J P; Zätterström U K; Kjellén E; Mertens F; Willén R; Mandahl N; Heim S; Mitelman F
Chromosomal abnormalities involving 11q13 are associated with poor prognosis in patients with squamous cell carcinoma of the head and neck.
Cancer 1995;76(5):853-9.
1995: Johansson B; Arheden K; Höglund M; Othzén A; Békássy A N; Turesson I; Heim S; Mitelman F
Fluorescence in situ hybridization analysis of whole-arm 7;12 translocations in hematologic malignancies.
Genes, chromosomes & cancer 1995;14(1):56-62.
1995: Panagopoulos I; Mandahl N; Mitelman F; Aman P
Two distinct FUS breakpoint clusters in myxoid liposarcoma and acute myeloid leukemia with the translocations t(12;16) and t(16;21).
Oncogene 1995;11(6):1133-7.
1995: Teixeira M R; Pandis N; Bardi G; Andersen J A; Mitelman F; Heim S
Clonal heterogeneity in breast cancer: karyotypic comparisons of multiple intra- and extra-tumorous samples from 3 patients.
International journal of cancer. Journal international du cancer 1995;63(1):63-8.
1995: Nilbert M; Rydholm A; Mitelman F; Meltzer P S; Mandahl N
Characterization of the 12q13-15 amplicon in soft tissue tumors.
Cancer genetics and cytogenetics 1995;83(1):32-6.
1995: Gorunova L; Johansson B; Dawiskiba S; Andrén-Sandberg A; Mandahl N; Heim S; Mitelman F
Cytogenetically detected clonal heterogeneity in a duodenal adenocarcinoma.
Cancer genetics and cytogenetics 1995;82(2):146-50.
1995: Johansson B; Waldenström J; Hasselblom S; Mitelman F
Waldenström's macroglobulinemia with the AML/MDS-associated t(1;3)(p36;q21).
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(7):1136-8.
1995: Jin Y; Mertens F; Jin C; Akervall J; Wennerberg J; Gorunova L; Mandahl N; Heim S; Mitelman F
Nonrandom chromosome abnormalities in short-term cultured primary squamous cell carcinomas of the head and neck.
Cancer research 1995;55(14):3204-10.
1995: Mertens F; Rydholm A; Bauer H F; Limon J; Nedoszytko B; Szadowska A; Willén H; Heim S; Mitelman F; Mandahl N
Cytogenetic findings in malignant peripheral nerve sheath tumors.
International journal of cancer. Journal international du cancer 1995;61(6):793-8.
1995: Mertens F; Heim S; Kullendorff C M; Donnér M; Hägerstrand I; Mitelman F; Mandahl N
Clonal karyotypic evolution in a pediatric neurofibrosarcoma.
Cancer genetics and cytogenetics 1995;81(2):135-8.
1995: Johansson M; Jin Y; Mandahl N; Hambraeus G; Johansson L; Mitelman F; Heim S
Cytogenetic analysis of short-term cultured squamous cell carcinomas of the lung.
Cancer genetics and cytogenetics 1995;81(1):46-55.
1995: Jin Y; Mertens F; Arheden K; Mandahl N; Wennerberg J; Dictor M; Heim S; Mitelman F
Karyotypic features of malignant tumors of the nasal cavity and paranasal sinuses.
International journal of cancer. Journal international du cancer 1995;60(5):637-41.
1995: Mertens F; Heim S; Mandahl N; Mitelman F; Brun A; Strömblad L G; Kullendorff C M; Donnér M
Recurrent chromosomal imbalances in choroid plexus tumors.
Cancer genetics and cytogenetics 1995;80(1):83-4.
1995: Pandis N; Jin Y; Gorunova L; Petersson C; Bardi G; Idvall I; Johansson B; Ingvar C; Mandahl N; Mitelman F
Chromosome analysis of 97 primary breast carcinomas: identification of eight karyotypic subgroups.
Genes, chromosomes & cancer 1995;12(3):173-85.
1995: Jin Y; Mertens F; Mandahl N; Wennerberg J; Dictor M; Heim S; Mitelman F
Tetraploidization and progressive loss of 6q in a squamous cell carcinoma of the parotid gland.
Cancer genetics and cytogenetics 1995;79(2):157-9.
1995: Aspberg F; Mertens F; Bauer H C; Lindholm J; Mitelman F; Mandahl N
Near-haploidy in two malignant fibrous histiocytomas.
Cancer genetics and cytogenetics 1995;79(2):119-22.
1995: Elfving P; Aman P; Mandahl N; Lundgren R; Mitelman F
Trisomy 7 in nonneoplastic epithelial kidney cells.
Cytogenetics and cell genetics 1995;69(1-2):90-6.
1995: Höglund M; Mitelman F; Mandahl N
A human 12p-derived cosmid hybridizing to subsets of human and chimpanzee telomeres.
Cytogenetics and cell genetics 1995;70(1-2):88-91.
1994: Panagopoulos I; Mandahl N; Ron D; Höglund M; Nilbert M; Mertens F; Mitelman F; Aman P
Characterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12;16 translocation.
Cancer research 1994;54(24):6500-3.
1994: Orndal C; Rydholm A; Willén H; Mitelman F; Mandahl N
Cytogenetic intratumor heterogeneity in soft tissue tumors.
Cancer genetics and cytogenetics 1994;78(2):127-37.
1994: Mertens F; Albert A; Heim S; Lindholm J; Brosjö O; Mitelman F; Mandahl N
Clonal structural chromosome aberrations in fibrous dysplasia.
Genes, chromosomes & cancer 1994;11(4):271-2.
1994: Panagopoulos I; Aman P; Fioretos T; Höglund M; Johansson B; Mandahl N; Heim S; Behrendtz M; Mitelman F
Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22).
Genes, chromosomes & cancer 1994;11(4):256-62.
1994: Gorunova L; Mertens F; Mandahl N; Jonsson N; Persson B; Heim S; Mitelman F
Cytogenetic heterogeneity in a clear cell hidradenoma of the skin.
Cancer genetics and cytogenetics 1994;77(1):26-32.
1994: Bardi G; Aman P; Johansson B; Pandis N; Mandahl N; Bak-Jensen E; Björkman A; Sjögren H O; Andrén-Sandberg A; Mitelman F
Cytogenetic characterization of a periampullary adenocarcinoma of the pancreas, its liver metastasis, and a cell line established from the metastasis and a cell line established from the metastasis in a patient with Gardner's syndrome.
Cancer genetics and cytogenetics 1994;76(1):29-32.
1994: Mertens F; Rydholm A; Brosjö O; Willén H; Mitelman F; Mandahl N
Hibernomas are characterized by rearrangements of chromosome bands 11q13-21.
International journal of cancer. Journal international du cancer 1994;58(4):503-5.
1994: Mertens F; Johansson B; Mitelman F
Isochromosomes in neoplasia.
Genes, chromosomes & cancer 1994;10(4):221-30.
1994: Jin Y; Mertens F; Limon J; Mandahl N; Wennerberg J; Dictor M; Heim S; Mitelman F
Characteristic karyotypic features in lacrimal and salivary gland carcinomas.
British journal of cancer 1994;70(1):42-7.
1994: Johansson B; Bardi G; Pandis N; Gorunova L; Bäckman P L; Mandahl N; Dawiskiba S; Andrén-Sandberg A; Heim S; Mitelman F
Karyotypic pattern of pancreatic adenocarcinomas correlates with survival and tumour grade.
International journal of cancer. Journal international du cancer 1994;58(1):8-13.
1994: Mertens F; Mandahl N; Mitelman F; Heim S
Cytogenetic analysis in the examination of solid tumors in children.
Pediatric hematology and oncology 1994;11(4):361-77.
1994: Johansson B; Mertens F; Mitelman F
Secondary chromosomal abnormalities in acute leukemias.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1994;8(6):953-62.
1994: Hagmar L; Brøgger A; Hansteen I L; Heim S; Högstedt B; Knudsen L; Lambert B; Linnainmaa K; Mitelman F; Nordenson I
Cancer risk in humans predicted by increased levels of chromosomal aberrations in lymphocytes: Nordic study group on the health risk of chromosome damage.
Cancer research 1994;54(11):2919-22.
1994: Johansson B; Billström R; Mauritzson N; Mitelman F
Trisomy 19 as the sole chromosomal anomaly in hematologic neoplasms.
Cancer genetics and cytogenetics 1994;74(1):62-5.
1994: Johansson M; Dietrich C; Mandahl N; Hambraeus G; Johansson L; Clausen P P; Mitelman F; Heim S
Karyotypic characterization of bronchial large cell carcinomas.
International journal of cancer. Journal international du cancer 1994;57(4):463-7.
1994: Mertens F; Kreicbergs A; Rydholm A; Willén H; Carlén B; Mitelman F; Mandahl N
Clonal chromosome aberrations in three sacral chordomas.
Cancer genetics and cytogenetics 1994;73(2):147-51.
1994: Nilbert M; Rydholm A; Willén H; Mitelman F; Mandahl N
MDM2 gene amplification correlates with ring chromosome in soft tissue tumors.
Genes, chromosomes & cancer 1994;9(4):261-5.
1994: Köhler M; Johansson B; Ludvigsson J; Aman P; Heim S; Mitelman F
Acute myeloid leukemia (AML-M1) with multiple trisomies and t(8;21)(q22;q22).
Cancer genetics and cytogenetics 1994;73(1):79-81.
1994: Mandahl N; Höglund M; Mertens F; Rydholm A; Willén H; Brosjö O; Mitelman F
Cytogenetic aberrations in 188 benign and borderline adipose tissue tumors.
Genes, chromosomes & cancer 1994;9(3):207-15.
1994: Nilbert M; Mandahl N; Aman P; Rydholm A; Mitelman F
No rearrangements of the CHOP gene in malignant fibrous histiocytoma.
Cancer genetics and cytogenetics 1994;72(2):155-6.
1994: Mertens F; Rydholm A; Kreicbergs A; Willén H; Jonsson K; Heim S; Mitelman F; Mandahl N
Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses.
Genes, chromosomes & cancer 1994;9(1):8-12.
1994: Mandahl N; Mertens F; Willén H; Rydholm A; Brosjö O; Mitelman F
A new cytogenetic subgroup in lipomas: loss of chromosome 16 material in spindle cell and pleomorphic lipomas.
Journal of cancer research and clinical oncology 1994;120(12):707-11.
1993: Johansson B; Mertens F; Mitelman F
Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci.
Genes, chromosomes & cancer 1993;8(4):205-18.
1993: Mertens F; Johansson B; Mitelman F
Age- and gender-related heterogeneity of cancer chromosome aberrations.
Cancer genetics and cytogenetics 1993;70(1):6-11.
1993: Aman P; Pejovic T; Wennborg A; Heim S; Mitelman F
Mapping of the 19p13 breakpoint in an ovarian carcinoma between the INSR and TCF3 loci.
Genes, chromosomes & cancer 1993;8(2):134-6.
1993: Bardi G; Johansson B; Pandis N; Mandahl N; Bak-Jensen E; Lindström C; Törnqvist A; Frederiksen H; Andrén-Sandberg A; Mitelman F
Cytogenetic analysis of 52 colorectal carcinomas--non-random aberration pattern and correlation with pathologic parameters.
International journal of cancer. Journal international du cancer 1993;55(3):422-8.
1993: Orndal C; Mandahl N; Willén H; Rydholm A; Mitelman F
Cytogenetic evolution in primary tumors, local recurrences, and pulmonary metastases of two soft tissue sarcomas.
Clinical & experimental metastasis 1993;11(5):401-8.
1993: Fioretos T; Nilsson P G; Aman P; Heim S; Kristoffersson U; Malm C; Simonsson B; Turesson I; Mitelman F
Clinical impact of breakpoint position within M-bcr in chronic myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1993;7(8):1225-31.
1993: Johansson M; Dietrich C; Mandahl N; Hambraeus G; Johansson L; Clausen P P; Mitelman F; Heim S
Recombinations of chromosomal bands 6p21 and 14q24 characterise pulmonary hamartomas.
British journal of cancer 1993;67(6):1236-41.
1993: Bardi G; Johansson B; Pandis N; Mandahl N; Bak-Jensen E; Andrén-Sandberg A; Mitelman F; Heim S
Karyotypic abnormalities in tumours of the pancreas.
British journal of cancer 1993;67(5):1106-12.
1993: Mandahl N; Orndal C; Heim S; Willén H; Rydholm A; Bauer H C; Mitelman F
Aberrations of chromosome segment 12q13-15 characterize a subgroup of hemangiopericytomas.
Cancer 1993;71(10):3009-13.
1993: Jin Y; Mertens F; Mandahl N; Heim S; Olegård C; Wennerberg J; Biörklund A; Mitelman F
Chromosome abnormalities in eighty-three head and neck squamous cell carcinomas: influence of culture conditions on karyotypic pattern.
Cancer research 1993;53(9):2140-6.
1993: Mertens F; Orndal C; Mandahl N; Heim S; Bauer H F; Rydholm A; Tufvesson A; Willén H; Mitelman F
Chromosome aberrations in tenosynovial giant cell tumors and nontumorous synovial tissue.
Genes, chromosomes & cancer 1993;6(4):212-7.
1993: Johansson B; Heim S; Mandahl N; Mertens F; Mitelman F
Trisomy 7 in nonneoplastic cells.
Genes, chromosomes & cancer 1993;6(4):199-205.
1993: Johansson M; Heim S; Mandahl N; Hambraeus G; Johansson L; Mitelman F
Cytogenetic analysis of six bronchial carcinoids.
Cancer genetics and cytogenetics 1993;66(1):33-8.
1993: Pandis N; Jin Y; Limon J; Bardi G; Idvall I; Mandahl N; Mitelman F; Heim S
Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast.
Genes, chromosomes & cancer 1993;6(3):151-5.
1993: Mandahl N; Baldetorp B; Fernö M; Akerman M; Rydholm A; Heim S; Willén H; Killander D; Mitelman F
Comparative cytogenetic and DNA flow cytometric analysis of 150 bone and soft-tissue tumors.
International journal of cancer. Journal international du cancer 1993;53(3):358-64.
1993: Mandahl N; Willén H; Rydholm A; Heim S; Mitelman F
Rearrangement of band q13 on both chromosomes 12 in a periosteal chondroma.
Genes, chromosomes & cancer 1993;6(2):121-3.
1993: Pejovic T; Heim S; Alm P; Iosif S; Himmelmann A; Skjaerris J; Mitelman F
Isochromosome 1q as the sole karyotypic abnormality in a Sertoli cell tumor of the ovary.
Cancer genetics and cytogenetics 1993;65(1):79-80.
1993: Bardi G; Johansson B; Pandis N; Bak-Jensen E; Orndal C; Heim S; Mandahl N; Andrén-Sandberg A; Mitelman F
Cytogenetic aberrations in colorectal adenocarcinomas and their correlation with clinicopathologic features.
Cancer 1993;71(2):306-14.
1993: Pandis N; Heim S; Bardi G; Idvall I; Mandahl N; Mitelman F
Chromosome analysis of 20 breast carcinomas: cytogenetic multiclonality and karyotypic-pathologic correlations.
Genes, chromosomes & cancer 1993;6(1):51-7.
1993: Orndal C; Mandahl N; Rydholm A; Willén H; Brosjö O; Mitelman F
Chromosome aberrations and cytogenetic intratumor heterogeneity in chondrosarcomas.
Journal of cancer research and clinical oncology 1993;120(1-2):51-6.
1993: Mitelman F
The cytogenetic scenario of chronic myeloid leukemia.
Leukemia & lymphoma 1993;11 Suppl 1():11-5.
1992: Aman P; Ron D; Mandahl N; Fioretos T; Heim S; Arheden K; Willén H; Rydholm A; Mitelman F
Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11).
Genes, chromosomes & cancer 1992;5(4):278-85.
1992: Johansson M; Jin Y; Heim S; Mandahl N; Hambraeus G; Johansson L; Mitelman F
Pseudodiploid karyotypes in adenosquamous carcinomas of the lung.
Cancer genetics and cytogenetics 1992;63(2):95-6.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Hägerstrand I; Holmin T; Andrén-Sandberg A; Mitelman F
Trisomy 7 in nonneoplastic focal steatosis of the liver.
Cancer genetics and cytogenetics 1992;63(1):22-4.
1992: Pandis N; Heim S; Bardi G; Idvall I; Mandahl N; Mitelman F
Whole-arm t(1;16) and i(1q) as sole anomalies identify gain of 1q as a primary chromosomal abnormality in breast cancer.
Genes, chromosomes & cancer 1992;5(3):235-8.
1992: Heim S; Mitelman F
Cytogenetic analysis in the diagnosis of acute leukemia.
Cancer 1992;70(6 Suppl):1701-9.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Bak-Jensen E; Frederiksen H; Andrén-Sandberg A; Mitelman F
Recurrent chromosome aberrations in abdominal smooth muscle tumors.
Cancer genetics and cytogenetics 1992;62(1):43-6.
1992: Fioretos T; Heim S; Garwicz S; Ludvigsson J; Mitelman F
Molecular analysis of Philadelphia-positive childhood chronic myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1992;6(7):723-5.
1992: Mitelman F; Heim S
Quantitative acute leukemia cytogenetics.
Genes, chromosomes & cancer 1992;5(1):57-66.
1992: Pandis N; Heim S; Bardi G; Limon J; Mandahl N; Mitelman F
Improved technique for short-term culture and cytogenetic analysis of human breast cancer.
Genes, chromosomes & cancer 1992;5(1):14-20.
1992: Olegård C; Mandahl N; Heim S; Willén H; Leifsson B; Mitelman F
Embryonal rhabdomyosarcoma with 100 chromosomes but no structural aberrations.
Cancer genetics and cytogenetics 1992;60(2):198-201.
1992: Orndal C; Mandahl N; Rydholm A; Willén H; Brosjö O; Heim S; Mitelman F
Supernumerary ring chromosomes in five bone and soft tissue tumors of low or borderline malignancy.
Cancer genetics and cytogenetics 1992;60(2):170-5.
1992: Orndal C; Mandahl N; Carlén B; Willén H; Wennerberg J; Heim S; Mitelman F
Near-haploid clones in a malignant fibrous histiocytoma.
Cancer genetics and cytogenetics 1992;60(2):147-51.
1992: Johansson B; Bardi G; Heim S; Mandahl N; Mertens F; Bak-Jensen E; Andrén-Sandberg A; Mitelman F
Nonrandom chromosomal rearrangements in pancreatic carcinomas.
Cancer 1992;69(7):1674-81.
1992: Mertens F; Jin Y; Heim S; Mandahl N; Jonsson N; Mertens O; Persson B; Salemark L; Wennerberg J; Mitelman F
Clonal structural chromosome aberrations in nonneoplastic cells of the skin and upper aerodigestive tract.
Genes, chromosomes & cancer 1992;4(3):235-40.
1992: Lundgren R; Heim S; Mandahl N; Anderson H; Mitelman F
Chromosome abnormalities are associated with unfavorable outcome in prostatic cancer patients.
The Journal of urology 1992;147(3 Pt 2):784-8.
1992: Pejovic T; Himmelmann A; Heim S; Mandahl N; Flodérus U M; Furgyik S; Elmfors B; Helm G; Willén H; Mitelman F
Prognostic impact of chromosome aberrations in ovarian cancer.
British journal of cancer 1992;65(2):282-6.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Andrén-Sandberg A; Hägerstrand I; Mitelman F
Cytogenetic findings in three primary hepatocellular carcinomas.
Cancer genetics and cytogenetics 1992;58(2):191-5.
1992: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Békássy A; Hägerstrand I; Mitelman F
Trisomy 2 as the sole chromosomal abnormality in a hepatoblastoma.
Genes, chromosomes & cancer 1992;4(1):78-80.
1992: Lundgren R; Mandahl N; Heim S; Limon J; Henrikson H; Mitelman F
Cytogenetic analysis of 57 primary prostatic adenocarcinomas.
Genes, chromosomes & cancer 1992;4(1):16-24.
1991: Bardi G; Pandis N; Mandahl N; Heim S; Sfikas K; Willén H; Panagiotopoulos G; Rydholm A; Mitelman F
Chromosomal abnormalities in giant cell tumors of bone.
Cancer genetics and cytogenetics 1991;57(2):161-7.
1991: Lindström E; Salford L G; Heim S; Mandahl N; Strömblad S; Brun A; Mitelman F
Trisomy 7 and sex chromosome loss need not be representative of tumor parenchyma cells in malignant glioma.
Genes, chromosomes & cancer 1991;3(6):474-9.
1991: Mertens F; Sallerfors B; Heim S; Johansson B; Kristoffersson U; Malm C; Mitelman F
Trisomy 13 as a primary chromosome aberration in acute leukemia.
Cancer genetics and cytogenetics 1991;56(1):39-44.
1991: Boldog F; Arheden K; Imreh S; Strömbeck B; Szekely L; Erlandsson R; Marcsek Z; Sumegi J; Mitelman F; Klein G
Involvement of 3p deletions in sporadic and hereditary forms of renal cell carcinoma.
Genes, chromosomes & cancer 1991;3(5):403-6.
1991: Pandis N; Heim S; Bardi G; Flodérus U M; Willén H; Mandahl N; Mitelman F
Chromosome analysis of 96 uterine leiomyomas.
Cancer genetics and cytogenetics 1991;55(1):11-8.
1991: Johansson B; Mertens F; Heim S; Kristoffersson U; Mitelman F
Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL).
European journal of haematology 1991;47(1):17-27.
1991: Bardi G; Johansson B; Pandis N; Heim S; Mandahl N; Andrén-Sandberg A; Hägerstrand I; Mitelman F
Trisomy 7 in short-term cultures of colorectal adenocarcinomas.
Genes, chromosomes & cancer 1991;3(2):149-52.
1991: Mertens F; Johansson B; Heim S; Kristoffersson U; Mitelman F
Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1991;5(3):214-20.
1991: Pejovic T; Heim S; Mandahl N; Elmfors B; Furgyik S; Flodérus U M; Helm G; Willén H; Mitelman F
Bilateral ovarian carcinoma: cytogenetic evidence of unicentric origin.
International journal of cancer. Journal international du cancer 1991;47(3):358-61.
1991: Mertens F; Heim S; Mandahl N; Johansson B; Mertens O; Persson B; Salemark L; Wennerberg J; Jonsson N; Mitelman F
Cytogenetic analysis of 33 basal cell carcinomas.
Cancer research 1991;51(3):954-7.
1991: Johansson B; Mertens F; Mitelman F
Geographic heterogeneity of neoplasia-associated chromosome aberrations.
Genes, chromosomes & cancer 1991;3(1):1-7.
1991: Higashi K; Jin Y; Johansson M; Heim S; Mandahl N; Biörklund A; Wennerberg J; Hambraeus G; Johansson L; Mitelman F
Rearrangement of 9p13 as the primary chromosomal aberration in adenoid cystic carcinoma of the respiratory tract.
Genes, chromosomes & cancer 1991;3(1):21-3.
1991: Orndal C; Carlén B; Akerman M; Willén H; Mandahl N; Heim S; Rydholm A; Mitelman F
Chromosomal abnormality t(9;22)(q22;q12) in an extraskeletal myxoid chondrosarcoma characterized by fine needle aspiration cytology, electron microscopy, immunohistochemistry and DNA flow cytometry.
Cytopathology : official journal of the British Society for Clinical Cytology 1991;2(5):261-70.
1990: Pandis N; Heim S; Bardi G; Flodérus U M; Willén H; Mandahl N; Mitelman F
Parallel karyotypic evolution and tumor progression in uterine leiomyoma.
Genes, chromosomes & cancer 1990;2(4):311-7.
1990: Rydholm A; Mandahl N; Heim S; Kreicbergs A; Willén H; Mitelman F
Malignant fibrous histiocytomas with a 19p+ marker chromosome have increased relapse rate.
Genes, chromosomes & cancer 1990;2(4):296-9.
1990: Pejovic T; Heim S; Orndal C; Jin Y S; Mandahl N; Willén H; Mitelman F
Simple numerical chromosome aberrations in well-differentiated malignant epithelial tumors.
Cancer genetics and cytogenetics 1990;49(1):95-101.
1990: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomas.
Human genetics 1990;85(6):605-11.
1990: Mandahl N; Heim S; Willén H; Rydholm A; Mitelman F
Supernumerary ring chromosome as the sole cytogenetic abnormality in a dermatofibrosarcoma protuberans.
Cancer genetics and cytogenetics 1990;49(2):273-5.
1990: Orndal C; Johansson M; Heim S; Mandahl N; Månsson B; Alumets J; Mitelman F
Parathyroid adenoma with t(1;5)(p22;q32) as the sole clonal chromosome abnormality.
Cancer genetics and cytogenetics 1990;48(2):225-8.
1990: Nilbert M; Mandahl N; Heim S; Rydholm A; Helm G; Willén H; Baldetorp B; Mitelman F
Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas.
Cancer genetics and cytogenetics 1990;48(2):217-23.
1990: Pandis N; Heim S; Bardi G; Mandahl N; Mitelman F
High resolution mapping of consistent leiomyoma breakpoints in chromosomes 12 and 14 to 12q15 and 14q24.1.
Genes, chromosomes & cancer 1990;2(3):227-30.
1990: Jin Y S; Higashi K; Mandahl N; Heim S; Wennerberg J; Biörklund A; Dictor M; Mitelman F
Frequent rearrangement of chromosomal bands 1p22 and 11q13 in squamous cell carcinomas of the head and neck.
Genes, chromosomes & cancer 1990;2(3):198-204.
1990: Johansson B; Mertens F; Heim S; Kristoffersson U; Mandahl N; Nilsson P G; Mitelman F
Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7).
Cancer genetics and cytogenetics 1990;48(1):119-23.
1990: Eneroth M; Mandahl N; Heim S; Willén H; Rydholm A; Alberts K A; Mitelman F
Localization of the chromosomal breakpoints of the t(12;16) in liposarcoma to subbands 12q13.3 and 16p11.2.
Cancer genetics and cytogenetics 1990;48(1):101-7.
1990: Johansson B; Mertens F; Fioretos T; Heim S; Kristoffersson U; Mandahl N; Bartram C R; Mitelman F
Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1990;4(6):448-9.
1990: Limon J; Lundgren R; Elfving P; Heim S; Kristoffersson U; Mandahl N; Mitelman F
An improved technique for short-term culturing of human prostatic adenocarcinoma tissue for cytogenetic analysis.
Cancer genetics and cytogenetics 1990;46(2):191-9.
1990: Pejovic T; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Complex karyotypic anomalies, including an i(5p) marker chromosome, in malignant mixed mesodermal tumor of the ovary.
Cancer genetics and cytogenetics 1990;46(1):65-9.
1990: Pejovic T; Heim S; Mandahl N; Elmfors B; Flodérus U M; Furgyik S; Helm G; Willén H; Mitelman F
Trisomy 12 is a consistent chromosomal aberration in benign ovarian tumors.
Genes, chromosomes & cancer 1990;2(1):48-52.
1990: Kristoffersson U; Heim S; Johnsson A; Mandahl N; Olsson H; Akerman M; Mitelman F
Deletion of 14q in non-Hodgkin's lymphoma.
European journal of haematology 1990;44(4):261-4.
1990: Heim S; Békàssy A N; Garwicz S; Heldrup J; Kristoffersson U; Mandahl N; Wiebe T; Mitelman F
Bone marrow karyotypes in 94 children with acute leukemia.
European journal of haematology 1990;44(4):227-33.
1990: Orndal C; Mandahl N; Rydholm A; Nilbert M; Heim S; Akerman M; Mitelman F
Chromosomal evolution and tumor progression in a myxoid liposarcoma.
Acta orthopaedica Scandinavica 1990;61(2):99-105.
1990: Brøgger A; Hagmar L; Hansteen I L; Heim S; Högstedt B; Knudsen L; Lambert B; Linnainmaa K; Mitelman F; Nordenson I
An inter-Nordic prospective study on cytogenetic endpoints and cancer risk. Nordic Study Group on the Health Risk of Chromosome Damage.
Cancer genetics and cytogenetics 1990;45(1):85-92.
1990: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Trisomy 12 in uterine leiomyomas. A new cytogenetic subgroup.
Cancer genetics and cytogenetics 1990;45(1):63-6.
1990: Mandahl N; Jin Y S; Heim S; Willén H; Wennerberg J; Biörklund A; Mitelman F
Trisomy 5 and loss of the Y chromosome as the sole cytogenetic anomalies in a cavernous hemangioma/angiosarcoma.
Genes, chromosomes & cancer 1990;1(4):315-6.
1990: Jin Y S; Heim S; Mandahl N; Biörklund A; Wennerberg J; Mitelman F
Multiple clonal chromosome aberrations in squamous cell carcinomas of the larynx.
Cancer genetics and cytogenetics 1990;44(2):209-16.
1990: Mandahl N; Heim S; Arheden K; Rydholm A; Willén H; Mitelman F
Chromosomal rearrangements in chondromatous tumors.
Cancer 1990;65(2):242-8.
1990: Nilbert M; Jin Y S; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Chromosome rearrangements in two uterine sarcomas.
Cancer genetics and cytogenetics 1990;44(1):27-35.
1990: Jin Y S; Heim S; Mandahl N; Biörklund A; Wennerberg J; Mitelman F
Unrelated clonal chromosomal aberrations in carcinomas of the oral cavity.
Genes, chromosomes & cancer 1990;1(3):209-15.
1990: Elfving P; Cigudosa J C; Lundgren R; Limon J; Mandahl N; Kristoffersson U; Heim S; Mitelman F
Trisomy 7, trisomy 10, and loss of the Y chromosome in short-term cultures of normal kidney tissue.
Cytogenetics and cell genetics 1990;53(2-3):123-5.
1990: Mitelman F; Heim S
Chromosome abnormalities in cancer.
Cancer detection and prevention 1990;14(5):527-37.
1989: Pejovic T; Heim S; Mandahl N; Elmfors B; Flodérus U M; Furgyik S; Helm G; Willén H; Mitelman F
Consistent occurrence of a 19p+ marker chromosome and loss of 11p material in ovarian seropapillary cystadenocarcinomas.
Genes, chromosomes & cancer 1989;1(2):167-71.
1989: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Baldetorp B; Mitelman F
Complex karyotypic anomalies in a bizarre leiomyoma of the uterus.
Genes, chromosomes & cancer 1989;1(2):131-4.
1989: Mandahl N; Heim S; Rydholm A; Willén H; Mitelman F
Structural chromosome aberrations in an adamantinoma.
Cancer genetics and cytogenetics 1989;42(2):187-90.
1989: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Different karyotypic abnormalities, t(1;6) and del(7), in two uterine leiomyomas from the same patient.
Cancer genetics and cytogenetics 1989;42(1):51-3.
1989: Mandahl N; Heim S; Brosjö O; Bauer H C; Tribukait B; Rydholm A; Mitelman F
Cytogenetic and quantitative DNA analysis of primary and xenografted human osteosarcomas.
Cancer genetics and cytogenetics 1989;42(1):27-34.
1989: Arheden K; Mandahl N; Heim S; Mitelman F
The INT1 oncogene is not rearranged or amplified in lipomas with structural chromosomal abnormalities of 12q13-15.
Cancer genetics and cytogenetics 1989;42(1):143-6.
1989: Mandahl N; Heim S; Willén H; Rydholm A; Eneroth M; Nilbert M; Kreicbergs A; Mitelman F
Characteristic karyotypic anomalies identify subtypes of malignant fibrous histiocytoma.
Genes, chromosomes & cancer 1989;1(1):9-14.
1989: Kristoffersson U; Heim S; Mandahl N; Akerman M; Mitelman F
Multiple clonal chromosome aberrations in two thymomas.
Cancer genetics and cytogenetics 1989;41(1):93-8.
1989: Lundgren R; Elfving P; Heim S; Kristoffersson U; Mandahl N; Mitelman F
A squamous cell bladder carcinoma with karyotypic abnormalities reminiscent of transitional cell carcinoma.
The Journal of urology 1989;142(2 Pt 1):374-6.
1989: Mertens F; Heim S; Mandahl N; Johansson B; Rydholm A; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Clonal chromosome aberrations in a keratoacanthoma and a basal cell papilloma.
Cancer genetics and cytogenetics 1989;39(2):227-32.
1989: Arheden K; Nilbert M; Heim S; Mandahl N; Mitelman F
No amplification or rearrangement of INT1, GLI, or COL2A1 in uterine leiomyomas with t(12;14)(q14-15;q23-24).
Cancer genetics and cytogenetics 1989;39(2):195-201.
1989: Limon J; Lundgren R; Elfving P; Heim S; Kristoffersson U; Mandahl N; Mitelman F
Double minutes in two primary adenocarcinomas of the prostate.
Cancer genetics and cytogenetics 1989;39(2):191-4.
1989: Heim S; Mertens F; Jin Y S; Mandahl N; Johansson B; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Diverse chromosome abnormalities in squamous cell carcinomas of the skin.
Cancer genetics and cytogenetics 1989;39(1):69-76.
1989: Jin Y S; Heim S; Mandahl N; Biörklund A; Wennerberg J; Willén R; Mitelman F
Two unrelated clonal chromosome rearrangements in a nasal papilloma.
Cancer genetics and cytogenetics 1989;39(1):29-34.
1989: Arheden K; Rønne M; Mandahl N; Heim S; Kinzler K W; Vogelstein B; Mitelman F
In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3-14.1.
Human genetics 1989;82(1):1-2.
1989: Brandt L; Kristoffersson U; Olsson H; Mitelman F
Relation between occupational exposure to organic solvents and chromosome aberrations in non-Hodgkin's lymphoma.
European journal of haematology 1989;42(3):298-302.
1989: Mertens F; Heim S; Jin Y S; Johansson B; Mandahl N; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Basosquamous papilloma. A benign epithelial skin tumor with multiple cytogenetic clones.
Cancer genetics and cytogenetics 1989;37(2):235-9.
1989: Nilbert M; Mandahl N; Heim S; Rydholm A; Willén H; Mitelman F
Cytogenetic abnormalities in an angioleiomyoma.
Cancer genetics and cytogenetics 1989;37(1):61-4.
1989: Heim S; Mitelman F
Cytogenetically unrelated clones in hematological neoplasms.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(1):6-8.
1989: Heim S; Mandahl N; Jin Y; Strömblad S; Lindström E; Salford L G; Mitelman F
Trisomy 7 and sex chromosome loss in human brain tissue.
Cytogenetics and cell genetics 1989;52(3-4):136-8.
1989: Heim S; Caron M; Jin Y; Mandahl N; Mitelman F
Genetic convergence during serial in vitro passage of a polyclonal squamous cell carcinoma.
Cytogenetics and cell genetics 1989;52(3-4):133-5.
1988: Jin Y; Heim J; Mandahl N; Biörklund A; Wennerberg J; Mitelman F
Inversion inv(4)(p15q26) in a squamous cell carcinoma of the hypopharynx.
Cancer genetics and cytogenetics 1988;36(2):233-4.
1988: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Akerman M; Mitelman F
Ring formation and structural rearrangements of chromosome 1 as secondary changes in uterine leiomyomas with t(12;14)(q14-15;q23-24).
Cancer genetics and cytogenetics 1988;36(2):183-90.
1988: Kristoffersson U; Heim S; Mandahl N; Olsson H; Akerman M; Mitelman F
Trisomy 5 and t(5;14)(q11;q32) as the sole abnormalities in two different clones from a centroblastic non-Hodgkin's lymphoma.
Cancer genetics and cytogenetics 1988;36(2):173-6.
1988: Heim S; Jin Y; Mandahl N; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Multiple unrelated clonal chromosome abnormalities in an in situ squamous cell carcinoma of the skin.
Cancer genetics and cytogenetics 1988;36(2):149-53.
1988: Heim S; Mandahl N; Rydholm A; Willén H; Mitelman F
Different karyotypic features characterize different clinico-pathologic subgroups of benign lipogenic tumors.
International journal of cancer. Journal international du cancer 1988;42(6):863-7.
1988: Mitelman F; Heim S
Consistent involvement of only 71 of the 329 chromosomal bands of the human genome in primary neoplasia-associated rearrangements.
Cancer research 1988;48(24 Pt 1):7115-9.
1988: Heim S; Mandahl N; Mitelman F
Genetic convergence and divergence in tumor progression.
Cancer research 1988;48(21):5911-6.
1988: Billström R; Thiede T; Hansen S; Heim S; Kristoffersson U; Mandahl N; Mitelman F
Bone marrow karyotype and prognosis in primary myelodysplastic syndromes.
European journal of haematology 1988;41(4):341-6.
1988: Heim S; Mandahl N; Arheden K; Giovanella B C; Yim S O; Stehlin J S; Mitelman F
Multiple karyotypic abnormalities, including structural rearrangements of 11p, in cell lines from malignant melanomas.
Cancer genetics and cytogenetics 1988;35(1):5-20.
1988: Lundgren R; Kristoffersson U; Heim S; Mandahl N; Mitelman F
Multiple structural chromosome rearrangements, including del(7q) and del(10q), in an adenocarcinoma of the prostate.
Cancer genetics and cytogenetics 1988;35(1):103-8.
1988: Nilbert M; Mandahl N; Heim S; Rydholm A; Willén H; Akerman M; Mitelman F
Chromosome abnormalities in leiomyosarcomas.
Cancer genetics and cytogenetics 1988;34(2):209-18.
1988: Karlsson I; Mandahl N; Heim S; Rydholm A; Willén H; Mitelman F
Complex chromosome rearrangements in an extraabdominal desmoid tumor.
Cancer genetics and cytogenetics 1988;34(2):241-5.
1988: Mertens F; Johansson B; Heim S; Mandahl N; Rydholm A; Mitelman F
Bands involved in primary chromosome rearrangements in sarcomas are not constitutionally liable to breakage in sarcoma patients.
Human genetics 1988;79(4):309-14.
1988: Mandahl N; Heim S; Arheden K; Rydholm A; Willén H; Mitelman F
Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas.
Human genetics 1988;79(3):203-8.
1988: Mertens F; Johansson B; Heim S; Mandahl N; Rydholm A; Mitelman F
Normal frequency of chromosome breakage in lymphocytes from patients with musculoskeletal sarcoma.
Cancer genetics and cytogenetics 1988;33(2):299-304.
1988: Mitelman F; Prigogina E L; Fleischman E W; Frenkel M A; Garwicz S; Heim S; Ilyinskaya G W; Kristoffersson U; Mandahl N; Volkova M A
A new specific chromosomal rearrangement, t(11;20)(p15;q11), in myeloblastic leukemia with maturation.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(7):430-2.
1988: Jin Y S; Mandahl N; Heim S; Schüller H; Mitelman F
Isochromosomes i(8q) or i(9q) in three adenocarcinomas of the lung.
Cancer genetics and cytogenetics 1988;33(1):11-7.
1988: Jin Y S; Mandahl N; Heim S; Biörklund A; Wennerberg J; Mitelman F
t(6;7)(q23;p22) as the sole chromosomal anomaly in a vocal cord carcinoma.
Cancer genetics and cytogenetics 1988;32(2):305-7.
1988: Mitelman F; Kolnig A M; Strömbeck B; Norrby R; Kromann-Andersen B; Sommer P; Wadstein J
No cytogenetic effects of quinolone treatment in humans.
Antimicrobial agents and chemotherapy 1988;32(6):936-7.
1988: Heim S; Nilbert M; Vanni R; Floderus U M; Mandahl N; Liedgren S; Lecca U; Mitelman F
A specific translocation, t(12;14)(q14-15;q23-24), characterizes a subgroup of uterine leiomyomas.
Cancer genetics and cytogenetics 1988;32(1):13-7.
1988: Jin Y S; Heim S; Mandahl N; Biörklund A; Wennerberg J; Mitelman F
Multiple apparently unrelated clonal chromosome abnormalities in a squamous cell carcinoma of the tongue.
Cancer genetics and cytogenetics 1988;32(1):93-100.
1988: Billström R; Nilsson P G; Mitelman F
Chromosomes, Auer rods and prognosis in acute myeloid leukaemia.
European journal of haematology 1988;40(3):273-8.
1988: Mandahl N; Heim S; Arheden K; Rydholm A; Willén H; Mitelman F
Multiple karyotypic rearrangements, including t(X;18)(p11;q11), in a fibrosarcoma.
Cancer genetics and cytogenetics 1988;30(2):323-7.
1988: Heim S; Kristoffersson U; Mandahl N; Malm C; Mitelman F
Variant translocation t(3;15)(q21;q22) in a patient with acute promyelocytic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(1):65-7.
1988: Jin Y S; Mandahl N; Heim S; Biörklund A; Wennerberg J; Mitelman F
Unique karyotypic abnormalities in a squamous cell carcinoma of the larynx.
Cancer genetics and cytogenetics 1988;30(1):177-9.
1988: Mandahl N; Heim S; Arheden K; Rydholm A; Willén H; Mitelman F
Rings, dicentrics, and telomeric association in histiocytomas.
Cancer genetics and cytogenetics 1988;30(1):23-33.
1988: Arheden K; Mandahl N; Strömbeck B; Isaksson M; Mitelman F
Chromosome localization of the human oncogene INT1 to 12q13 by in situ hybridization.
Cytogenetics and cell genetics 1988;47(1-2):86-7.
1988: Nilbert M; Heim S; Mandahl N; Flodérus U M; Willén H; Mitelman F
Karyotypic rearrangements in 20 uterine leiomyomas.
Cytogenetics and cell genetics 1988;49(4):300-4.
1988: Arheden K; Tommerup N; Mandahl N; Heim S; Winther J; Jensen O A; Prause J U; Mitelman F
Amplification of the human putative oncogene INT1 in primary retinoblastoma tumors.
Cytogenetics and cell genetics 1988;48(3):174-7.
1987: Heim S; Alimena G; Billström R; Diverio D; Kristoffersson U; Mandahl N; Nanni M; Mitelman F
Tetraploid karyotype (92,XXYY) in two patients with acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1987;29(1):129-33.
1987: Billström R; Nilsson P G; Mitelman F
Characteristic patterns of chromosome abnormalities in acute myeloid leukemia with Auer rods.
Cancer genetics and cytogenetics 1987;28(2):191-9.
1987: Billström R; Nilsson P G; Mitelman F
Normal bone marrow karyotype in acute leukemia or myelodysplasia following rheumatoid arthritis?
Cancer genetics and cytogenetics 1987;25(1):161-4.
1987: Heim S; Békàssy A N; Garwicz S; Heldrup J; Wiebe T; Kristoffersson U; Mandahl N; Mitelman F
New structural chromosomal rearrangements in congenital leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1987;1(1):16-23.
1986: Billström R; Nilsson P G; Mitelman F
Cytogenetic analysis in 941 consecutive patients with haematologic disorders.
Scandinavian journal of haematology 1986;37(1):29-40.
1986: Hedner K; Kolnig A M; Strömbeck B; Nordén A; Mitelman F
A twin study of structural chromosome aberrations in lymphocytes.
Cytogenetics and cell genetics 1986;41(1):58-9.
1985: Heim S; Billström R; Kristoffersson U; Mandahl N; Strömbeck B; Mitelman F
Variant Ph translocations in chronic myeloid leukemia.
Cancer genetics and cytogenetics 1985;18(3):215-27.
1984: Hedner K; Mitelman F; Pero R W
Sister-chromatid exchanges in human lymphocytes after a non-S-phase incubation period to allow excision DNA repair-in vitro exposure to N-acetoxy-2-acetylaminofluorene and ethylene oxide.
Mutation research 1984;129(1):71-6.
1984: Hedner K; Iselius L; Mitelman F; Nordén A; Pero R W
A twin study of sister chromatid exchanges in human lymphocytes following carcinogen exposure and DNA repair incubation.
Cytogenetics and cell genetics 1984;38(3):189-91.
1984: Brøgger A; Norum R; Hansteen I L; Clausen K O; Skårdal K; Mitelman F; Kolnig A M; Strömbeck B; Nordenson I; Andersson G
Comparison between five Nordic laboratories on scoring of human lymphocyte chromosome aberrations.
Hereditas 1984;100(2):209-18.
1983: Hedner K; Högstedt B; Kolnig A M; Mark-Vendel E; Strömbeck B; Mitelman F
Sister chromatid exchanges and structural chromosome aberrations in relation to smoking in 91 individuals.
Hereditas 1983;98(1):77-81.
1983: Högstedt B; Gullberg B; Hedner K; Kolnig A M; Mitelman F; Skerfving S; Widegren B
Chromosome aberrations and micronuclei in bone marrow cells and peripheral blood lymphocytes in humans exposed to ethylene oxide.
Hereditas 1983;98(1):105-13.
1982: Hedner K; Högstedt B; Kolnig A M; Mark-Vendel E; Strömbeck B; Mitelman F
Sister chromatid exchanges and structural chromosome aberrations in relation to age and sex.
Human genetics 1982;62(4):305-9.
1982: Hedner K; Högstedt B; Kolnig A M; Mark-Vendel E; Strömbeck B; Mitelman F
Relationship between sister chromatid exchanges and structural chromosome aberrations in lymphocytes of 100 individuals.
Hereditas 1982;97(2):237-45.
1981: Pero R W; Widegren B; Högstedt B; Mitelman F
In vivo and in vitro ethylene oxide exposure of human lymphocytes assessed by chemical stimulation of unscheduled DNA synthesis.
Mutation research 1981;83(2):271-89.
1981: Mark-Vendel E; Högstedt B; Skerfving S; Mitelman F
Location of chromosome aberrations in bone marrow cells of individuals exposed mainly to petroleum vapors.
Hereditas 1981;95(2):235-7.
1981: Högstedt B; Gullberg B; Mark-Vendel E; Mitelman F; Skerfving S
Micronuclei and chromosome aberrations in bone marrow cells and lymphocytes of humans exposed mainly to petroleum vapors.
Hereditas 1981;94(2):179-87.
1980: Högstedt B; Kolnig A M; Mitelman F; Skerfving S
Cytogenetic study of pesticides in agricultural work.
Hereditas 1980;92(1):177-8.

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