Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3

Nature Genetics

Volumn 11, Issue 3, 1995, Pages 338-340

  Pronk, Jan C ^a   Gibson, Rachel A ^b   Savoia, Anna ^c   Wijker, Mario ^a   Morgan, Neil V ^b   Melchionda, Salvatore ^c   Ford, Deborah ^d   Temtamy, Samia ^e   Ortega, Juan J ^f   Jansen, Stander ^g   Havenga, Charmaine ^g   Cohn, Richard J ^h   de Ravel, Thomy J ^h   Roberts, Irene ⁱ   Westerveld, Andries ^j   Easton, Douglas F ^d   Joenje, Hans ^a   Mathew, Christopher G ^b   Arwert, Fré ^a  

^a VU UNIVERSITY AMSTERDAM   (Netherlands)

^b GUY S HOSPITAL   (United Kingdom)

^c IRCCS San Giovanni Rotondo   (Italy)

^d INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^e NATIONAL RESEARCH CENTRE   (Egypt)

^f HOSPITAL MATERNO INFANTIL VALL D HEBRON   (Spain)

^g UNIVERSITY OF THE FREE STATE   (South Africa)

^h UNIVERSITY OF THE WITWATERSRAND   (South Africa)

ⁱ HAMMERSMITH HOSPITAL   (United Kingdom)

^j UNIVERSITY OF AMSTERDAM   (Netherlands)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CELL LINE; CHROMOSOME 16Q; CHROMOSOME MARKER; FAMILY STUDY; FANCONI ANEMIA; FEMALE; GENE LOCUS; GENE MAPPING; GENETIC COMPLEMENTATION; GENETIC LINKAGE; HOMOZYGOSITY; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 20; CONSANGUINITY; FANCONI ANEMIA; GENETIC COMPLEMENTATION TEST; HUMAN; LINKAGE (GENETICS); PEDIGREE; SUPPORT, NON-U.S. GOV'T;

EID: 0028840709     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1195-338     Document Type: Article

References (18)

1. Liu, J.M., Buchwald, M., Walsh, C.E. & Young, N.S. Fanconi anaemia and novel strategies for therapy. Blood 84, 3995-4007 (1994).
2. Strathdee, C.A., Duncan, A.M.V. & Buchwald, M. Evidence for at least 4 Fanconi anaemia genes including FACC on chromosome 9. Nature Genet. 1, 196-198 (1992).
3. Joenje, H. et al. Classification of Fanconi anaemia patients by complementation analysis: evidence for a fifth genetic subtype. Blood (in the press).
4. Joenje, H. for EUFAR. Assignment of Fanconi anaemia patients to complementation groups: an update. Acta Haematologica 93, 250 (1995).
5. Strathdee, C.A., Gavish, H., Shannon, W.R. & Buchwald, M. Cloning of cDNAs for Fanconi’s anaemia by functional complementation. Nature 356, 763-767 (1992). Correction: 358; 434 (1992).
6. Mann, W.R. et al. Fanconi anaemia - evidence for linkage heterogeneity on chromosome 20q. Genomics 9, 329-337 (1991).
7. Dogget, N.A. & Callen, D.F. Report of the third international workshop on human chromosome 16 mapping 1994. Cytogenet. Cell Genet. 68, 166-177 (1995).
8. Gyapay, G. et al. The 1993-94 Généthon human genetic linkage map. Nature Genet. 7, 246-339 (1994).
9. Jorde, L.B. Linkage disequilibrium as a gene-mapping tool. Am. J. hum. Genet. 56, 11-14 (1995).
10. Rosendorff, J., Bernstein, R., Macdougall, L. & Jenkins, T. Fanconi anaemia: another disease of high prevalence in the Afrikaans population of South Africa. Am. J. med. Genet.27, 793-797 (1987).
11. Duckworth-Rysiecki, G., Cornish, K., Clarke, C.A. & Buchwald, M. Identification of two complementation groups in Fanconi anaemia. Somatic Cell molec. Genet. 11, 35-41 (1985).
12. Savitsky, K. et al. A single ataxia telangiectasia gene with a product similar to PIS kinase.Science 268, 1749-1753 (1995).
13. Auerbach, A.D., Rogatko, A. & Schroeder-Kurth, T.M., International Fanconi anaemia Registry: Relation of clinical symptoms to diepoxybutane sensitivity. Blood 73, 391-396 (1989).
14. Litt, M. & Luty, A.L. A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene. Am. J. hum. Genet. 44, 397-401 (1989).
15. Reed, P. et al. Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping. Nature Genet. 7, 390-395 (1994).
16. Nikali, K. et al. Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus. Am. J. hum. Genet. 56, 1088-1095 (1995).
17. Lathrop, G.M., Lalouel, J.M., Julier, C. & Ott, J. Strategies for multilocus linkage analysis in humans. Proc. natn. Acad. Sci. U.S.A. 81, 3443-3446 (1984).
18. Bengtsson, B.O. & Thomson, G. Measuring the strength of associations between HLA antigens and diseases. Tissue Antigens 18, 356-363 (1981).