Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

Inherited loss-of-function mutations in the tumor suppressor genes BRCA1, BRCA2, and multiple other genes predispose to high risks of breast and/or ovarian cancer. Cancer-associated inherited mutations in these genes are collectively quite common, but individually rare or even private. Genetic testi...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Walsh, Tom, Lee, Ming K., Casadei, Silvia, Thornton, Anne M., Stray, Sunday M., Pennil, Christopher, Nord, Alex S., Mandell, Jessica B., Swisher, Elizabeth M., King, Mary-Claire
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: National Academy of Sciences 2010
Gaiak:
Biological Sciences
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2906584/
https://ncbi.nlm.nih.gov/pubmed/20616022
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1007983107
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