Genomic profiling of breast tumours in relation to BRCA abnormalities and phenotypes

INTRODUCTION: Germline mutations in the BRCA1 and BRCA2 genes account for a considerable fraction of familial predisposition to breast cancer. Somatic mutations in BRCA1 and BRCA2 have not been found and the involvement of these genes in sporadic tumour development therefore remains unclear. METHODS...

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Detalles Bibliográficos
Autores principales: Stefansson, Olafur Andri, Jonasson, Jon Gunnlaugur, Johannsson, Oskar Thor, Olafsdottir, Kristrun, Steinarsdottir, Margret, Valgeirsdottir, Sigridur, Eyfjord, Jorunn Erla
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750106/
https://www.ncbi.nlm.nih.gov/pubmed/19589159
http://dx.doi.org/10.1186/bcr2334

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750106/
https://www.ncbi.nlm.nih.gov/pubmed/19589159
http://dx.doi.org/10.1186/bcr2334

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