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PMID: 1598904 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Closing in on a breast cancer gene on chromosome 17q.

American journal of human genetics ·Vol. 50 ·No. 6 ·1992-06-00 ·Pages 1235-42

Hall JM, Friedman L, Guenther C, Lee MK, Weber JL, Black DM, King MC

Abstract

Linkage of early-onset familial breast and ovarian cancer to 11 markers on chromosome 17q12-q21 defines an 8-cM region which is very likely to include the disease gene BRCA 1. The most closely linked marker is D17S579, a highly informative CA repeat polymorphism. D17S579 has no recombinants with inherited breast or ovarian cancer in 79 informative meioses in the seven families with early-onset disease (lod score 9.12 at zero recombination). There is no evidence for linkage heterogeneity in the families with early-onset disease. The proportion of older-onset breast cancer attributable to BRCA 1 is not yet determinable, because both inherited and sporadic cases occur in older-onset families.

Related Genes
MeSH Terms
Base Sequence Breast Neoplasms/genetics Chromosome Banding Chromosomes, Human, Pair 17 Female Genetic Linkage Genetic Markers Haplotypes Humans Male Molecular Sequence Data Oligodeoxyribonucleotides Ovarian Neoplasms/genetics Pedigree Polymorphism, Genetic Repetitive Sequences, Nucleic Acid Restriction Mapping
Chemicals
Genetic Markers Oligodeoxyribonucleotides
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Hall J M
School of Public Health, University of California, Berkeley 94720.
Friedman L
Guenther C
Lee M K
Weber J L
Black D M
King M C
References (14)
14 references, click to expand
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1992-06-00
Pages
1235-42
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1682570
Subset
IM
Grants
NCI NIH HHS · CA27632 · United States
NHGRI NIH HHS · HG00248 · United States
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