Integrated Evaluation of DNA Sequence Variants of Unknown Clinical Significance: Application to BRCA1 and BRCA2-Reference-Cited by-同舟云学术

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Integrated Evaluation of DNA Sequence Variants of Unknown Clinical Significance: Application to BRCA1 and BRCA2

Published:2004-10 Issue:4 Volume:75 Page:535-544
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Goldgar David E.,Easton Douglas F.,Deffenbaugh Amie M.,Monteiro Alvaro N.A.,Tavtigian Sean V.,Couch Fergus J.

Funder

Medical Research and Materiel Command

National Institutes of Health

Canadian Institutes of Health Research

Breast Cancer Research Foundation

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference25 articles.

1. Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation;Abkevich;J Med Genet,2004

2. Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies;Antoniou;Am J Hum Genet,2003

3. BRCA1 R841W: a strong candidate for a common mutation with moderate phenotype;Barker;Genet Epidemiol,1996

4. Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases;Breast Cancer Linkage Consortium;Lancet,1997

5. Expression of BRC repeats in breast cancer cells disrupts the BRCA2-Rad51 complex and leads to radiation hypersensitivity and loss of G(2)/M checkpoint control;Chen;J Biol Chem,1999

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