Prevalence of BRCA1 and BRCA2 Mutations in Patients with Primary Ovarian Cancer – Does the German Checklist for Detecting the Risk of Hereditary Breast and Ovarian Cancer Adequately Depict the Need for Consultation?

Background BRCA1/2 mutations are the leading cause of hereditary epithelial ovarian cancer (EOC). The German Consortium for Hereditary Breast and Ovarian Cancer has defined inclusion criteria, which are retrievable as a checklist and facilitate genetic counselling/testing for affected persons with a...

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Detalles Bibliográficos
Autores principales: Ataseven, Beyhan, Tripon, Denise, Rhiem, Kerstin, Harter, Philipp, Schneider, Stephanie, Heitz, Florian, Baert, Thais, Traut, Alexander, Pauly, Nina, Ehmann, Sarah, Plett, Helmut, Schmutzler, Rita K., du Bois, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467803/
https://www.ncbi.nlm.nih.gov/pubmed/32905297
http://dx.doi.org/10.1055/a-1222-0042

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467803/
https://www.ncbi.nlm.nih.gov/pubmed/32905297
http://dx.doi.org/10.1055/a-1222-0042

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