Username

Password

Forgot Password?

Preview

Sign-in free and Explore the Exciting World of BiomedExperts:

Over 1.500.000 Profiles
More than 1.800 Organizations worldwide
State of the Art Network Visualizations

Manage your own Profile
Locate Experts in your Country/Region
Locate Experts in your 1. and 2. Level Network
Connect to Experts Worldwide

NetworkView

Hon Fong Mark

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.

Research Profile (preview)

Procedures

Anatomy

Disorders

Occupations

Cytogenetics

Genes & Molecular Sequences

erbB-2 Genes

Physiology

Chemicals & Drugs

DNA Probes

Concepts & Ideas

Metaphase

Sign-in to see full Profile

Network (preview)

Co-Publications
Name
13
Santoro, K
11
Samy, M
9
Mark, S
8
Afify, Alaa
8
Lathrop, JC
7
Bland, KI
7
Sotomayor, Edgar
7
Sun, CL
6
Zolnierz, K
5
Taylor, W
5
Das, S
5
Feldman, D
5
Rintels, P
4
Brown, S
4
Gray, Y

Sign-in to see all Coauthors

Publications

TOP 3
Mark Hon Fong L
Dr. R. J. McKinlay Gardner Interviewed by Dr. Hon Fong L. Mark.
Sotomayor Edgar A; Shah Inangati M; Sanger Warren G; Mark Hon Fong L
In situ follicular lymphoma with a 14;18 translocation diagnosed by a multimodal approach.
Mechoso Búrix; Vaglio Alicia; Quadrelli Andrea; Mark Hon Fong L; Huang Xin-Li; Milunsky Aubrey; Quadrelli Roberto
A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.

Sign-in to see all Publications

Sign in free and see...

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the visualized research activity
of experts around the globe

Sign-in to see more

Geonetwork of Hon Fong Mark (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

Sign-in to see more

All Publications

2008: Mark Hon Fong L
Dr. R. J. McKinlay Gardner Interviewed by Dr. Hon Fong L. Mark.
Journal of the Association of Genetic Technologists 2008;34(1):9-10.
2007: Sotomayor Edgar A; Shah Inangati M; Sanger Warren G; Mark Hon Fong L
In situ follicular lymphoma with a 14;18 translocation diagnosed by a multimodal approach.
Experimental and molecular pathology 2007;83(2):254-8.
2007: Mechoso Búrix; Vaglio Alicia; Quadrelli Andrea; Mark Hon Fong L; Huang Xin-Li; Milunsky Aubrey; Quadrelli Roberto
A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.
Fetal diagnosis and therapy 2007;22(4):249-53.
2006: Mark Hon Fong L; Sotomayor Edgar A; Nelson Marilu; Chaves Fernando; Sanger Warren G; Kaleem Zahid; Caughron Samuel K
Chronic idiopathic myelofibrosis (CIMF) resulting from a unique 3;9 translocation disrupting the janus kinase 2 (JAK2) gene.
Experimental and molecular pathology 2006;81(3):217-23.
2006: Hayne Cynthia C; Winer Eric; Williams Tara; Chaves Fernando; Khorsand Jila; Mark Hon Fong L
Acute lymphoblastic leukemia with 4;11 translocation analyzed by a multi-modal strategy of conventional cytogenetics, FISH, morphology, flow cytometry and molecular genetics, and review of the literature.
Experimental and molecular pathology 2006;81(1):62-71.
2006: Mark Hon Fong L; Sokolic Robert A; Mark Yvonne
Conventional cytogenetics and FISH in the detection of BCR/ABL fusion in chronic myeloid leukemia (CML).
Experimental and molecular pathology 2006;81(1):1-7.
2006: Wyandt Herman E; Shim Sung Han; Mark Hon Fong L; Huang Xin Li; Milunsky Jeff M
Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
Experimental and molecular pathology 2006;80(3):262-6.
2006: Tonk Vijay; Wilson Golder; Schutt Robert; Mock Justin; Wyandt Herman; Mark Hon Fong L; Ito Masamichi
Costovertebral dysplasia in a patient with partial trisomy 22.
Experimental and molecular pathology 2006;80(2):197-200.
2005: Huang X-L; de Michelena M I; Mark H F L; Harston R; Benke P J; Price S J; Milunsky A
Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
Clinical genetics 2005;68(6):513-9.
2005: Mark Hon Fong L; Wyandt Herman; Pan Agen; Milunsky Jeff M
Constitutional partial 1q trisomy mosaicism and Wilms tumor.
Cancer genetics and cytogenetics 2005;162(2):166-71.
2005: Mark H F L; Wyandt H; Huang X L; Milunsky J M
Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
Clinical genetics 2005;68(2):146-51.
2000: Mark H F; Caldarone R; Colt A; Viner-Brown S I; Zimmerman A; Simon P
Public health genetics in Rhode Island: first steps.
Medicine and health, Rhode Island 2000;83(6):191-2.
2000: Bearer E L; Chen A F; Chen A H; Li Z; Mark H F; Smith R J; Jackson C L
2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4.
Annals of human genetics 2000;64(Pt 3):189-96.
2000: Mark H F; Bai H; Sotomayor E; Mark S; Rintels P
Hypotetraploidy in a patient with small cell carcinoma.
Experimental and molecular pathology 2000;68(1):70-6.
2000: Mark H F; Samy M; Santoro K; Mark S; Feldman D
Fluorescent in situ hybridization study of c-myc oncogene copy number in prostate cancer.
Experimental and molecular pathology 2000;68(1):65-9.
2000: Persons D L; Bui M M; Lowery M C; Mark H F; Yung J F; Birkmeier J M; Wong E Y; Yang S J; Masood S
Fluorescence in situ hybridization (FISH) for detection of HER-2/neu amplification in breast cancer: a multicenter portability study.
Annals of clinical and laboratory science 2000;30(1):41-8.
1999: Sokolic R A; Ferguson W; Mark H F
Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemia.
Cancer genetics and cytogenetics 1999;115(2):106-13.
1999: Mark H F; Feldman D; Das S; Samy M; Sun C L; Mark S
Assessment of chromosomal trisomies in prostate cancer using fluorescent in situ hybridization.
Experimental and molecular pathology 1999;67(2):109-17.
1999: Mark H F; Sigman M
Male infertility associated with a unique 8;22 translocation.
Experimental and molecular pathology 1999;67(1):57-61.
1999: Mark H F; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
Experimental and molecular pathology 1999;67(1):50-6.
1999: Mark H F; Sotomayor E; Mega A
Occurrence of both t(1;19) and t(8;14) in a patient with chronic lymphocytic leukemia.
Experimental and molecular pathology 1999;66(3):238-42.
1999: Mark H F; Feldman D; Das S; Kye H; Mark S; Sun C L; Samy M
Fluorescence in situ hybridization study of HER-2/neu oncogene amplification in prostate cancer.
Experimental and molecular pathology 1999;66(2):170-8.
1999: Afify A M; Werness B A; Mark H F
HER-2/neu oncogene amplification in stage I and stage III ovarian papillary serous carcinoma.
Experimental and molecular pathology 1999;66(2):163-9.
1999: Mark H F; Feldman D; Samy M; Sun C; Das S; Mark S; Lathrop J
Assessment of chromosome 8 copy number in cervical cancer by fluorescent in situ hybridization.
Experimental and molecular pathology 1999;66(2):157-62.
1999: Mark H F
Conventional and molecular cytogenetics in medicine.
Medicine and health, Rhode Island 1999;82(5):160-3.
1999: Mark H F; Afify A M; Werness B A; Das S; Mark S; Samy M
Trisomy 8 in stage I and stage III ovarian cancer detected by fluorescence in situ hybridization.
Experimental and molecular pathology 1999;66(1):76-81.
1999: Mark H F; Aswad B; Bassily N; Taylor W; Brown S; Sun C L; Samy M; Zolnierz K; Wong E; Bland K I; Hsu P H
HER-2/neu gene amplification in stages I-IV breast cancer detected by fluorescent in situ hybridization.
Genetics in medicine : official journal of the American College of Medical Genetics 1999;1(3):98-103.
1999: Mark H F; Alter D; Mousseau P
Klinefelter syndrome.
Archives of pathology & laboratory medicine 1999;123(3):261.
1999: Mark H F; Gray Y; Sotomayor E; Joseph P
Trisomy 9 in a patient with secondary acute myelogenous leukemia detected by fluorescent in situ hybridization.
Pathobiology : journal of immunopathology, molecular and cellular biology 1999;67(2):111-4.
1999: Mark H F; Gray Y; Mark Y; Khorsand J; Sikov W
A multimodal approach in the diagnosis of patients with hematopoietic disorders.
Cancer genetics and cytogenetics 1999;109(1):14-20.
1999: Estalilla O; Rintels P; Mark H F
Trisomy 10 as a sole chromosomal abnormality in AML-M2.
Cancer genetics and cytogenetics 1999;108(2):175.
1999: Afify A; Mark H F
Trisomy 8 in embryonal rhabdomyosarcoma detected by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1999;108(2):127-32.
1999: Mark H F; Brown S; Taylor W; Bassily N; Sun C L; Samy M; Bland K I
Study of chromosome 12 copy number in breast cancer using fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1999;108(1):26-31.
1999: Mark H F; Taylor W; Brown S; Samy M; Sun C L; Santoro K; Bland K I
Abnormal chromosome 8 copy number in stage I to stage IV breast cancer studied by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1999;108(1):1-5.
1999: Mark H F; Feldman D; Das S; Sun C L; Samy M; Lathrop J
HER-2/neu oncogene amplification in cervical cancer studied by fluorescent in situ hybridization.
Genetic testing 1999;3(2):237-42.
1999: Mark H F; Feldman D; Sigman M
Conventional and molecular cytogenetic identification of a variant klinefelter syndrome patient with a deleted X chromosome.
Pathobiology : journal of immunopathology, molecular and cellular biology 1999;67(1):55-8.
1998: Mark H F; Alter D N; Mega A
FISH as an adjunct to conventional cytogenetics.
Medicine and health, Rhode Island 1998;81(10):328-30.
1998: Masood S; Bui M M; Yung J F; Mark H F; Wong E Y; Birkmeier J M; Yang S J; Hsu P
Reproducibility of LSI HER-2/neu SpectrumOrange and CEP 17 SpectrumGreen Dual Color deoxyribonucleic acid probe kit. For enumeration of gene amplification in paraffin-embedded specimens: a multicenter clinical validation study.
Annals of clinical and laboratory science 1998;28(4):215-23.
1998: Mark H F; McCarthy M; Berry D
Advances in breast cancer genetics.
Medicine and health, Rhode Island 1998;81(5):183-6.
1998: Mark H F; Rehan J; Mark S; Santoro K; Zolnierz K
Fluorescence in situ hybridization analysis of single-cell trisomies for determination of clonality.
Cancer genetics and cytogenetics 1998;102(1):1-5.
1998: Mark H F; Wells L
A laboratorian's view on the College of American Pathologists' Laboratory Accreditation Program for Clinical Laboratories.
Annals of clinical and laboratory science 1998;28(2):115-23.
1998: Estalilla O; Rintels P; Mark H F
Trisomy 10 in leukemia.
Cancer genetics and cytogenetics 1998;101(1):68-71.
1998: Mark H F; Rausch M E; Taylor W M; Huth A; Mark S; Santoro K; Zolnierz K; Ferreira K; Barker B E
Sequential flow cytometry and fluorescence in situ hybridization for the study of formalin-fixed, paraffin-embedded breast cancer cells.
Cancer genetics and cytogenetics 1998;100(2):129-33.
1998: Mark H F; Mark Y; Sotomayor E; Sambandam S
A patient with myelodysplastic syndrome studied by GTG-banding and fluorescent in situ hybridization (FISH).
Cytobios 1998;94(376):121-8.
1998: Mark H F; Przygoda J J; Sikov W
Fluorescent in situ hybridization for identifying cytogenetic abnormalities in inadequate and suboptimal specimens.
Pathobiology : journal of immunopathology, molecular and cellular biology 1998;66(5):216-20.
1998: Mark H F; Brown S; Sun C L; Samy M; Afify A
Fluorescent in situ hybridization detection of HER-2/neu gene amplification in rhabdomyosarcoma.
Pathobiology : journal of immunopathology, molecular and cellular biology 1998;66(2):59-63.
1997: Mark H F; Afify A; Taylor W; Santoro K; Lathrop J C
A subset of gestational trophoblastic disease characterized by abnormal chromosome 8 copy number detected by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1997;99(1):24-9.
1997: Afify A; Mark H F
Fluorescence in situ hybridization assessment of chromosome 8 copy number in stage I and stage II infiltrating ductal carcinoma of the breast.
Cancer genetics and cytogenetics 1997;97(2):101-5.
1997: Mark H F; Bier J A
Disappearing trisomy 8 mosaicism.
Annals of clinical and laboratory science 1997;27(4):293-8.
1997: Mark H F; Mills D R; Santoro K; Quddus M R; Lathrop J C
Fluorescent in situ hybridization analysis of cervical smears. A pilot study of 20 cases.
Annals of clinical and laboratory science 1997;27(3):224-9.
1997: Mark H F; Jenkins R; Miller W A
Current applications of molecular cytogenetic technologies.
Annals of clinical and laboratory science 1997;27(1):47-56.
1997: Chang S S; Mark H F
Emerging molecular cytogenetic technologies.
Cytobios 1997;90(360):7-22.
1997: Mark H F; Gray Y; Rintels P
Translocation 2;19 in a patient with probable relapsed acute myeloid leukemia.
Pathobiology : journal of immunopathology, molecular and cellular biology 1997;65(4):223-8.
1997: Mark H F; Taylor W; Afify A; Riera D; Rausch M; Huth A; Gray Y; Santoro K; Bland K I
Stage I and stage II infiltrating ductal carcinoma of the breast analyzed for chromosome 8 copy number using fluorescent in situ hybridization.
Pathobiology : journal of immunopathology, molecular and cellular biology 1997;65(4):184-9.
1996: Nebres M V; Mark H F
Breast cancer among Asian women.
Medicine and health, Rhode Island 1996;79(11):388-91.
1996: Mark H F
The detection of translocations using chromosome painting for monitoring exposure to potential genotoxicants.
Medicine and health, Rhode Island 1996;79(9):333-5.
1996: Mark H F; Annas G; Ricker R; Weitzel J
Clinical and research issues in breast cancer genetics.
Annals of clinical and laboratory science 1996;26(5):396-408.
1996: Mark H F; Hanna I; Gnepp D R
Cytogenetic analysis of salivary gland type tumors.
Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics 1996;82(2):187-92.
1996: Mark H F; Bier J A; Scola P
The frequency of chromosomal abnormalities in patients referred for fragile X analysis.
Annals of clinical and laboratory science 1996;26(4):323-8.
1996: Young C; Di Benedetto J; Glasser L; Mark H F
A Philadelphia chromosome positive CML patient with a unique translocation studied via GTG-banding and fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1996;89(2):157-62.
1996: Mark H F; Naram R; Singer J; Rice R; LaMarche P H
Douglas-fir: a third wood-drying condensate found to exhibit in vitro cytotoxicity and genotoxicity.
Annals of clinical and laboratory science 1996;26(3):269-74.
1996: Wu C D; Medeiros L J; Miranda R N; Mark H F; Rintels P
Chronic myeloid leukemia manifested during megakaryoblastic crisis.
Southern medical journal 1996;89(4):422-7.
1996: Mark H F; Santoro K; Campbell W; Hann E; Lathrop J
Integration of human papillomavirus sequences in cervical tumor cell lines.
Annals of clinical and laboratory science 1996;26(2):147-53.
1996: Mark H F; Lathrop J
Cytogenetics in obstetrics and gynecology.
Medicine and health, Rhode Island 1996;79(2):55-7.
1996: Mark H F; Bland K I
Laboratory study of breast cancer using conventional and molecular cytogenetics.
Medicine and health, Rhode Island 1996;79(2):50-4.
1996: Mark H F; Bayleran J K; Seifer D B; Meyers-Seifer C H
A combined cytogenetic and molecular approach for diagnosing delayed puberty.
Clinical pediatrics 1996;35(2):62-6.
1996: Mark H F; Naram R; Singer J T; Rice R W; Bastan W C; Beauregard L J; Lamarche P H
Wood-drying condensate from Eastern white pine induced cytotoxicity and genotoxicity in vitro.
Annals of clinical and laboratory science 1996;26(1):64-70.
1996: Mark H F; Prence E; Beauregard L; Greenstein R
The impact of managed care on genetic testing laboratories in the United States.
Cytobios 1996;88(352):43-52.
1996: Mark H F; McGowan K D
Issues in the genetic assessment of predispositions for familial breast and ovarian cancer.
Cytobios 1996;87(351):229-35.
1996: Mark H F; Mills D R; Kim E; Santoro K; Quddus M R; Lathrop J C
Fluorescent in situ hybridization assessment of chromosome copy number in buccal mucosal cells.
Cytobios 1996;87(349):117-26.
1996: Mark H F; Dong Y H; Forman E; Smith P; Glasser L
A multimodal approach for diagnosing patients with acute promyelocytic leukaemia.
Cytobios 1996;87(350):137-49.
1996: Afify A; Bland K I; Mark H F
Fluorescent in situ hybridization assessment of chromosome 8 copy number in breast cancer.
Breast cancer research and treatment 1996;38(2):201-8.
1995: Mark H F; Chow B K
Localization of the gene encoding the secretin receptor, SCTR, on human chromosome 2q14.1 by fluorescence in situ hybridization and chromosome morphometry.
Genomics 1995;29(3):817-8.
1995: Mark H F; Kelly T; Watson M S; Hoeltge G; Miller W A; Beauregard L
Current issues of personnel and laboratory practices in genetic testing.
Journal of medical genetics 1995;32(10):780-6.
1995: Mark H F; Meyers-Seifer C H; Seifer D B; Demoranville B M; Jackson I M
Assessment of sex chromosome composition using fluorescent in situ hybridization as an adjunct to GTG-banding.
Annals of clinical and laboratory science 1995;25(5):402-8.
1995: Mark H F; Sikov W; Safran H; King T C; Griffith R C
Fluorescent in situ hybridization for assessing the proportion of cells with trisomy 4 in a patient with acute non-lymphoblastic leukemia.
Annals of clinical and laboratory science 1995;25(4):330-5.
1995: Mark H F; Grollino M G; Sulaiman R A; Lathrop J C
Fluorescent in situ hybridization assessment of chromosome copy number in gestational trophoblastic disease.
Annals of clinical and laboratory science 1995;25(4):291-6.
1995: Mark H F; Naram R; Singer J T; Rice R W; Bastan B; Beauregard L J; LaMarche P H
Cytotoxicity and genotoxicity of wood drying condensate from Southern Yellow Pine: an in vitro study.
Mutation research 1995;342(3-4):191-6.
1995: Abuelo D; Mark H F; Bier J A
Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization.
Clinical pediatrics 1995;34(4):223-6.
1995: Mark H F; Hann E; Mikumo R; Lauchlan S; Beauregard L; Braun L
Cytogenetic characterization of three cell lines derived from primary cervical tumors.
Annals of clinical and laboratory science 1995;25(2):185-99.
1995: Mark H F; Naram R; Bastan W C; Cherkes J K; LaMarche P H
Red oak condensate: its apparent lack of cytotoxic and genotoxic effects as compared with three other wood-drying condensates.
Cytobios 1995;84(338-339):133-40.
1995: Mark H F; Naram R; Santoro K; Bland K I
A study of induced genotoxicity in MCF-7 cells.
Cytobios 1995;84(338-339):171-7.
1995: Mark H F; Naram R; Singer J T; Rice R W; Bastan B; Beauregard L J; LaMarche P H
Eastern white pine wood-drying condensate induced cytotoxicity and genotoxicity in human peripheral blood lymphocytes in vitro.
Cytobios 1995;83(332):25-31.
1995: Mark H F; Sheu M; Lopes L; Campagnone J; Takezawa K; Santoro K; Sigman M
Towards the development of a fluorescent in situ hybridization based genotoxicologic assay for aneuploidy detection in sperm.
Cytobios 1995;82(330):171-80.
1994: Miranda R N; Mark H F; Medeiros L J
Fluorescent in situ hybridization in routinely processed bone marrow aspirate clot and core biopsy sections.
The American journal of pathology 1994;145(6):1309-14.
1994: Mark H F; Gnepp D R; Nigri P; Campbell W; Mark Y
Combined strategy of conventional cytogenetics, fluorescent in situ hybridization and chromosome morphometry for analysis of parotid gland tumor.
Annals of clinical and laboratory science 1994;24(6):555-9.
1994: Mark H F
Recent advances in molecular cytogenetics: fluorescent in situ hybridization.
Rhode Island medicine 1994;77(11):377-81.
1994: Mark H F; Naram R; Pham T; Shah K; Cousens L P; Wiersch C; Airall E; Samy M; Zolnierz K; Mark R
A practical cytogenetic protocol for in vitro cytotoxicity and genotoxicity testing.
Annals of clinical and laboratory science 1994;24(5):387-95.
1994: Miranda R N; Mark H F; Oyer C E
Sudden infant death syndrome (SIDS)
Pediatric pathology / affiliated with the International Paediatric Pathology Association 1994;14(4):751-4.
1994: Mark H F
Fluorescent in situ hybridization as an adjunct to conventional cytogenetics.
Annals of clinical and laboratory science 1994;24(2):153-63.
1993: Mark H F; Wyandt H E; Pan T; Mark R; Paramenter M; Campbell W; Mark Y
A study of homologous chromosomes using a morphometric approach.
Genome / National Research Council Canada = Génome / Conseil national de recherches Canada 1993;36(5):1003-6.
1993: Braun L; Mikumo R; Mark H F; Lauchlan S
Analysis of the growth properties and physical state of the human papillomavirus type 16 genome in cell lines derived from primary cervical tumors.
The American journal of pathology 1993;143(3):832-44.
1993: Mark H F; Mark R; Pan T; Mark Y
Centromere index derivation by a novel and convenient approach.
Annals of clinical and laboratory science 1993;23(4):267-74.
1993: Mark H F; Parmenter M; Campbell W; Mark R; Zolnierz K; Dunwoodie D; Hann E; Airall E; Santoro K; Mark Y
A novel, convenient, and inexpensive approach for deriving ISCN (1985) relative lengths: validation by a morphometric study of 100 karyotyped metaphase cells.
Cytogenetics and cell genetics 1993;62(1):13-8.
1992: Jackson C L; Britt D E; Graw S L; Potts A; Santoro K; Buckler A J; Housman D E; Mark H F
Construction and characterization of radiation hybrids for chromosome 9, and their use in mapping cosmid probes on the chromosome.
Somatic cell and molecular genetics 1992;18(3):285-301.
1992: Hansen K; Bagtas J; Mark H F; Homans A; Singer D B
Undifferentiated small cell hepatoblastoma with a unique chromosomal translocation: a case report.
Pediatric pathology / affiliated with the International Paediatric Pathology Association 1992;12(3):457-62.

Sign-in to see more