Rates of BRCA1/2 mutation testing among young survivors of breast cancer-Reference-Cited by-同舟云学术

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Rates of BRCA1/2 mutation testing among young survivors of breast cancer

Published:2015-12-26 Issue:1 Volume:155 Page:165-173
ISSN:0167-6806
Container-title:Breast Cancer Research and Treatment
language:en
Short-container-title:Breast Cancer Res Treat

Author:

Kehl Kenneth L.,Shen Chan,Litton Jennifer K.,Arun Banu,Giordano Sharon H.

Funder

Duncan Family Institute

Baker Institute for Health and Biosciences

Cancer Prevention Research Institute of Texas

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology

Link

http://link.springer.com/content/pdf/10.1007/s10549-015-3658-y.pdf

Reference36 articles.

1. Foulkes WD (2008) Inherited susceptibility to common cancers. N Engl J Med 359:2143–2153. doi: 10.1056/NEJMra0802968

2. Pharoah PDP, Antoniou A, Bobrow M et al (2002) Polygenic susceptibility to breast cancer and implications for prevention. Nat Genet 31:33–36. doi: 10.1038/ng853

3. Antoniou A, Pharoah PDP, Narod S et al (2003) 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. Am J Hum Genet 72:1117–1130. doi: 10.1086/375033

4. National comprehensive cancer network. Genetic/familial high-risk screening: breast. Version 1.2001

5. National comprehensive cancer network. Genetic/familial high-risk assessment: breast and ovarian. Version 1.2005

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