Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing-Reference-Cited by-同舟云学术

Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

Published:2010-06-28 Issue:28 Volume:107 Page:12629-12633
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proc Natl Acad Sci USA

Author:

Walsh Tom,Lee Ming K.,Casadei Silvia,Thornton Anne M.,Stray Sunday M.,Pennil Christopher,Nord Alex S.,Mandell Jessica B.,Swisher Elizabeth M.,King Mary-Claire

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference33 articles.

1. Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2

2. Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

3. PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

4. Beyond Li Fraumeni Syndrome: Clinical Characteristics of Families With p53 Germline Mutations

5. Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancer

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