BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives
- 1 May 2006
- journal article
- Published by Elsevier in European Journal Of Cancer
- Vol. 42 (8) , 1143-1150
- https://doi.org/10.1016/j.ejca.2005.11.032
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Prediction of pathogenic mutations in patients with early-onset breast cancer by family historyThe Lancet, 2003
- Family History of Breast and Ovarian Cancers and BRCA1 and BRCA2 Mutations in a Population-Based Series of Early-Onset Breast CancerJNCI Journal of the National Cancer Institute, 2001
- Low prevalence of germline BRCA1 mutations in early onset breast cancer without a family historyJournal of Medical Genetics, 2000
- Prevalence of BRCA1 and BRCA2 Gene Mutations in Patients With Early-Onset Breast CancerJNCI Journal of the National Cancer Institute, 1999
- Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer FamiliesAmerican Journal of Human Genetics, 1998
- The genetics of inherited breast cancer.Journal of Mammary Gland Biology and Neoplasia, 1998
- Differential Contributions ofBRCA1andBRCA2to Early-Onset Breast CancerNew England Journal of Medicine, 1997
- Germ-LineBRCA1Mutations in Jewish and Non-Jewish Women with Early-Onset Breast CancerNew England Journal of Medicine, 1996
- Rapid Detection of Translation-Terminating Mutations at the Adenomatous Polyposis Coli (APC) Gene by Direct Protein Truncation TestGenomics, 1994
- Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.Proceedings of the National Academy of Sciences, 1989