A breast-ovarian cancer susceptibility gene maps to chromosome 17q21

Am J Hum Genet. 1993 Apr;52(4):736-42.

Abstract

Nineteen North American Caucasian families that contain a minimum of four confirmed cases of breast or ovarian cancer have been studied. Four polymorphisms (cLB17.1, D17S579, D17S588, and D17S74), which span a region of approximately 15 cM on chromosome 17q12, were typed. Our data confirm the location of a dominant gene conferring susceptibility to breast and ovarian cancer (maximum lod = 9.78) and suggest that the breast-ovarian cancer syndrome is genetically heterogeneous. Two recombinants in one large family suggest that the breast-ovarian cancer locus lies between D17S588 and D17S579.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Breast Neoplasms / genetics*
  • Canada
  • Chromosome Mapping / methods*
  • Chromosomes, Human, Pair 17*
  • Family Health
  • Female
  • Gene Expression
  • Genes, Dominant
  • Genetic Linkage
  • Genetic Markers
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Lod Score
  • Male
  • Middle Aged
  • Neoplastic Syndromes, Hereditary
  • Ovarian Neoplasms / genetics*
  • Pedigree
  • Polymorphism, Genetic
  • Proto-Oncogenes*
  • Recombination, Genetic
  • United States

Substances

  • Genetic Markers