Skip to main content
American Journal of Human Genetics logoLink to American Journal of Human Genetics
letter
. 1997 Dec;61(6):1454–1456. doi: 10.1086/301631

Meiotic microdeletion breakpoints in the BRCA1 gene are significantly associated with symmetric DNA-sequence elements.

B Schmucker, M Krawczak
PMCID: PMC1716079  PMID: 9399889

Full text

PDF
1454

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Krawczak M., Cooper D. N. Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment. Hum Genet. 1991 Mar;86(5):425–441. doi: 10.1007/BF00194629. [DOI] [PubMed] [Google Scholar]
  2. Smith G. R. Chi hotspots of generalized recombination. Cell. 1983 Oct;34(3):709–710. doi: 10.1016/0092-8674(83)90525-1. [DOI] [PubMed] [Google Scholar]
  3. Struewing J. P., Brody L. C., Erdos M. R., Kase R. G., Giambarresi T. R., Smith S. A., Collins F. S., Tucker M. A. Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer. Am J Hum Genet. 1995 Jul;57(1):1–7. [PMC free article] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES