Copy Number Variation Analysis in Familial BRCA1/2-Negative Finnish Breast and Ovarian Cancer

BACKGROUND: 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 in the Finnish popu...

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Detalles Bibliográficos
Autores principales: Kuusisto, Kirsi M., Akinrinade, Oyediran, Vihinen, Mauno, Kankuri-Tammilehto, Minna, Laasanen, Satu-Leena, Schleutker, Johanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742470/
https://www.ncbi.nlm.nih.gov/pubmed/23967248
http://dx.doi.org/10.1371/journal.pone.0071802

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742470/
https://www.ncbi.nlm.nih.gov/pubmed/23967248
http://dx.doi.org/10.1371/journal.pone.0071802

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