Molecular analysis of the six most recurrent mutations in the BRCA1 gene in 87 Spanish breast/ovarian cancer families
- 30 January 1998
- journal article
- Published by Elsevier in Cancer Letters
- Vol. 123 (2) , 153-158
- https://doi.org/10.1016/s0304-3835(97)00416-3
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- The 12 base pair duplication/insertion alteration could be a regulatory mutation.Journal of Medical Genetics, 1997
- BRCA1Mutations in a Population-Based Sample of Young Women with Breast CancerNew England Journal of Medicine, 1996
- Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlationNature Genetics, 1995
- The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsNature Genetics, 1995
- A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screeningPublished by American Medical Association (AMA) ,1995
- Common origins of BRCA1 mutations in Canadian breast and ovarian cancer familiesNature Genetics, 1994
- A P1-based physical map of the region from D17S776 to D17S78 containing the breast cancer susceptibility gene BRCA1Human Molecular Genetics, 1994
- A Strong Candidate for the Breast and Ovarian Cancer Susceptibility Gene BRCA1Science, 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