Evaluation of the need for routine clinical testing of PALB2 c.1592delT mutation in BRCA negative Northern Finnish breast cancer families

BACKGROUND: Testing for mutations in the BRCA1 and BRCA2 genes among high-risk breast cancer patients has become a routine practice among clinical geneticists. Unfortunately, however, the genetic background of a majority of the cases coming to the clinics remains currently unexplained, making geneti...

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Detalles Bibliográficos
Autores principales: Haanpää, Maria, Pylkäs, Katri, Moilanen, Jukka S, Winqvist, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751431/
https://www.ncbi.nlm.nih.gov/pubmed/23941127
http://dx.doi.org/10.1186/1471-2350-14-82

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751431/
https://www.ncbi.nlm.nih.gov/pubmed/23941127
http://dx.doi.org/10.1186/1471-2350-14-82

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