Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer
Purpose To characterise the prevalence of pathogenic germline mutations in BRCA1 and BRCA2 in families with breast cancer (BC) and ovarian cancer (OC) history. Patients and methods Data from 21 401 families were gathered between 1996 and 2014 in a clinical setting in the German Consortium for Heredi...
|Published in:||Journal of medical genetics, 53(2016), 7, Seite 465-471|
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29 February 2016
|Item Description:||Gesehen am 12.03.2018|
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