Reassignment of MYCL1 to human chromosome 1p34.3 by fluorescence in situ hybridization

Cytogenetics and Cell Genetics

Volumn 72, Issue 2-3, 1996, Pages 189-190

  Speleman, F ^a   Van Camp, G ^b   Van Roy, N ^a  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

^b UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 1P; FLUORESCENCE IN SITU HYBRIDIZATION; GENE ASSIGNMENT; GENE LOCATION; HUMAN; HUMAN CELL; MYELOID LEUKEMIA; ONCOGENE; ONCOGENE MYC; PRIORITY JOURNAL;

CHROMOSOMES, HUMAN, PAIR 1; GENES, MYC; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE;

EID: 0029924654     PISSN: 03010171     EISSN: 1424859X     Source Type: Journal    
DOI: 10.1159/000134185     Document Type: Article

References (11)

1. Coucke P, Van Camp G, Djoyodiharjo B, Smith SD, Frants RR, Padberg GW. Darby JR. Huizing EH, Cromers CWRJ, Kimherling WJ, Ooslra BA, Van de Heyning PH, Willems PJ: Linkage of autosomal dominant hearing loss to the short arm of chromosome I in two families. New Engl J Med 331:425-431 (1994).
2. Dracopoli NC, O'Connell P, Eisner TL, Lalouel J-M, While RL, Buetow KH, Nishimura DY. Murray JC. Helms C, Mishra SK, Donis-Kelter H, Hall JM, Lee MK, King M-C. Attwood J, Morton NE, Robson F.B, Mahlani M, Willard HF. Royle NJ, Patel I. Jeffreys AJ, Verga V. Jenkins T. Weber JL, Mitchell AL, Bale AE: The CEPH consortium linkage map of human chromosome I. Genomies 9: 686-700(1991).
3. Fong C. While PS, Peterson K, Sapicnza C, Cavenee WK, Kern SE, Vogelstein B, Cantor AB, Look AT. Brodeur GM: Loss of heterozygosity for chromosomes 1 or 14 defines subsets of advanced neuroblastomas. Cancer Res 52:1780-1785 (1992).
4. Hellslen E, Vesa J, Speer MC. Mäkelä TP, Jarvela I. Alilalo K, Ott J, Pcltonen L: Refined assignment of the infantile neuronal ceroid lipofuscinosis (1NCL, CLNI) locus al Ip32: incorporation of linkage disequilibrium in multipoint analysis. Genomics 16:720-725(1993).
5. Hellsten E, Vesa J, Heiskanen M, Makela TP, Jarvela I. Cowell JK, Mead S, Alilalo K, Palotie A, Peltonen L: Identification of YAC clones for human chromosome Ip32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locus. Genomics 25:404-412 (1995).
6. Matise T. Perlin M, Chakravarti A: Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage maP, Nature Gcnciics 6:384-390 (1994).
7. Nau MM, Brooks BJ, Batley J, Sausville E, Gazdar AF. Kirsch IR. McBride OW. Bertness V. Hollis GF. Minna JD: L-myc. a new mir-related gene amplified and expressed in human small cell lung cancer. Nature 318:69-73 (1985).
8. Schleierrracher G, Peter M, Michon J, Hugot JP, Vielh P, Zucker JM, Magdclenat H, Thomas G, Delattre O: Two distinct deleted regions on the short arm of chromosome 1 in neuroblastomA, Genes Chrom Cancer 10:275-281 (1994).
9. Takeda O. Homma C. Maseki N. Sakurai M, Kanda N. Schwab M, Nakamura Y. Kaneko Y: There may be two tumor suppressor genes on chromosome arm I p closely associated with biologically distinct sub-types of neuroblastomA, Genes Chrom Cancer 10:30-39 (1994).
10. Van Roy N. Laureys G, Vcrsleeg R. Opdenakker G, Spelcman F: High resolution mapping of 46 DNA markers to the short arm of human chromosome I. Genomics 18:71-78(1993).
11. Van Roy N, Cheng NC. Laureys G, Opdenakker G, Versleeg R. Spoleman F: Molecular cytogenetic analysis of 1:17 translocations in neuroblastomA, Eurj Cancer 3IA:530-535 (1995).