Molecular profiles of BRCA1-mutated and matched sporadic breast tumours: relation with clinico-pathological features

About 5–10% of breast cancers are hereditary; a genetically and clinically heterogeneous disease in which several susceptibility genes, including BRCA1, have been identified. While distinct tumour features can be used to estimate the likelihood that a breast tumour is caused by a BRCA1 germline muta...

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Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Berns, E M J J, Staveren, I L van, Verhoog, L, Ouweland, A M W van de, Gelder, M Meijer-van, Meijers-Heijboer, H, Portengen, H, Foekens, J A, Dorssers, L C J, Klijn, J G M
Materialtyp: Artigo
Språk:Inglês
Publicerad: Nature Publishing Group 2001
Ämnen:
Regular Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2364107/
https://ncbi.nlm.nih.gov/pubmed/11506493
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1054/bjoc.2001.1937
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