copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.

copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.

<h4>Background</h4>Inherited factors predisposing individuals to breast and ovarian cancer are largely unidentified in a majority of families with hereditary breast and ovarian cancer (HBOC). We aimed to identify germline copy number variations (CNVs) contributing to HBOC susceptibility...

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Bibliographic Details
Main Authors: Kirsi M Kuusisto, Oyediran Akinrinade, Mauno Vihinen, Minna Kankuri-Tammilehto, Satu-Leena Laasanen, Johanna Schleutker
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23967248/?tool=EBI

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https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23967248/?tool=EBI

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