RNA profiling reveals familial aggregation of molecular subtypes in non-BRCA1/2 breast cancer families

BACKGROUND: In more than 70% of families with a strong history of breast and ovarian cancers, pathogenic mutation in BRCA1 or BRCA2 cannot be identified, even though hereditary factors are expected to be involved. It has been proposed that tumors with similar molecular phenotypes also share similar...

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Detalles Bibliográficos
Autores principales: Larsen, Martin J, Thomassen, Mads, Tan, Qihua, Lænkholm, Anne-Vibeke, Bak, Martin, Sørensen, Kristina P, Andersen, Mette Klarskov, Kruse, Torben A, Gerdes, Anne-Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909442/
https://www.ncbi.nlm.nih.gov/pubmed/24479546
http://dx.doi.org/10.1186/1755-8794-7-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909442/
https://www.ncbi.nlm.nih.gov/pubmed/24479546
http://dx.doi.org/10.1186/1755-8794-7-9

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