Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families
- 1 December 1994
- journal article
- research article
- Published by Springer Nature in Nature Genetics
- Vol. 8 (4), 392-398
- https://doi.org/10.1038/ng1294-392
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Linkage analysis of 26 Canadian breast and breast-ovarian cancer familiesHuman Genetics, 1995
- A P1-based physical map of the region from D17S776 to D17S78 containing the breast cancer susceptibility gene BRCA1Human Molecular Genetics, 1994
- BRCA1 Mutations in Primary Breast and Ovarian CarcinomasScience, 1994
- Localization of a Breast Cancer Susceptibility Gene, BRCA2 , to Chromosome 13q12-13Science, 1994
- A Large Kindred With 17q-Linked Breast and Ovarian Cancer: Genetic, Phenotypic, and Genealogical AnalysisJNCI Journal of the National Cancer Institute, 1994
- High-Density Genetic Map of the BRCA1 Region of Chromosome 17q12-q21Genomics, 1993
- Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12–21: exclusion of candidate genes EDH17B2 and RARAHuman Molecular Genetics, 1993
- A suggested nomenclature for designating mutationsHuman Mutation, 1993
- Familial breast-ovarian cancer locus on chromosome 17q12-q23The Lancet, 1991
- Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21Science, 1990