The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation?-Reference-Cited by-同舟云学术

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The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation?

Published:2013-09-12 Issue:5 Volume:84 Page:407-414
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Hilbers FSM¹,Vreeswijk MPG¹²,van Asperen CJ³,Devilee P¹⁴

Affiliation:

1. Department of Human Genetics; Leiden University Medical Centre; Leiden The Netherlands

2. Department of Toxicogenetics; Leiden University Medical Centre; Leiden The Netherlands

3. Department of Clinical Genetics; Leiden University Medical Centre; Leiden The Netherlands

4. Department of Pathology; Leiden University Medical Centre; Leiden The Netherlands

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference90 articles.

1. Familial breast cancer;Lalloo;Clin Genet,2012

2. Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases;Anglian Breast Cancer Study Group;Br J Cancer,2000

3. How many more breast cancer predisposition genes are there?;Easton;Breast Cancer Res,1999

4. Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer;Peto;J Natl Cancer Inst,1999

5. Breast Cancer infromation Core http://research.nhgri.nih.gov/projects/bic/index.shtml

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