Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results

Author:

Pritzlaff Mary,Summerour Pia,McFarland Rachel,Li Shuwei,Reineke Patrick,Dolinsky Jill S.,Goldgar David E.,Shimelis Hermela,Couch Fergus J.,Chao Elizabeth C.,LaDuca Holly

Funder

National Cancer Institute

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology

Reference38 articles.

1. The NCCN Clinical Practice Guidelines in Oncology™ Genetic/Familial High-Risk Assessment: Breast and Ovarian V2.2016. National Comprehensive Cancer Network, Inc. 2016. http://www.nccn.org/ . Accessed 22 Sept 2016

2. Thorlacius S, Sigurdsson S, Bjarnadottir H et al (1997) Study of a single BRCA2 mutation with high carrier frequency in a small population. Am J Hum Genet 60(5):1079–1084

3. Couch FJ, Faird LM, SeSHano ML et al (1996) BRCA2 germline mutations in male breast cancer cases and breast cancer families. Nat Genet 13(1):123–125

4. Frank TS, Deffenbaugh AM, Reid JE et al (2002) Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals. J Clin Oncol 20(6):1480–1490

5. Kwong A, Ng EK, Wong CL et al (2012) Identification of BRCA1/2 founder mutations in Southern Chinese breast cancer patients using gene sequencing and high resolution DNA melting analysis. PLoS ONE 7(9):e43994

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