Use of DNA–Damaging Agents and RNA Pooling to Assess Expression Profiles Associated with BRCA1 and BRCA2 Mutation Status in Familial Breast Cancer Patients

A large number of rare sequence variants of unknown clinical significance have been identified in the breast cancer susceptibility genes, BRCA1 and BRCA2. Laboratory-based methods that can distinguish between carriers of pathogenic mutations and non-carriers are likely to have utility for the classi...

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Detalles Bibliográficos
Autores principales: Walker, Logan C., Thompson, Bryony A., Waddell, Nic, Investigators, kConFab, Grimmond, Sean M., Spurdle, Amanda B.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2824809/
https://www.ncbi.nlm.nih.gov/pubmed/20174566
http://dx.doi.org/10.1371/journal.pgen.1000850

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2824809/
https://www.ncbi.nlm.nih.gov/pubmed/20174566
http://dx.doi.org/10.1371/journal.pgen.1000850

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