Contribution of large genomic BRCA1 alterations to early-onset breast cancer selected for family history and tumour morphology: a report from The Breast Cancer Family Registry

INTRODUCTION: Selecting women affected with breast cancer who are most likely to carry a germline mutation in BRCA1 and applying the most appropriate test methodology remains challenging for cancer genetics services. We sought to test the value of selecting women for BRCA1 mutation testing on the ba...

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Autori principali: Smith, Letitia D, Tesoriero, Andrea A, Wong, Ee M, Ramus, Susan J, O'Malley, Frances P, Mulligan, Anna Marie, Terry, Mary Beth, Senie, Ruby T, Santella, Regina M, John, Esther M, Andrulis, Irene L, Ozcelik, Hilmi, Daly, Mary B, Godwin, Andrew K, Buys, Saundra S, Fox, Stephen, Goldgar, David E, Giles, Graham G, Hopper, John L, Southey, Melissa C
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2011
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3109582/
https://ncbi.nlm.nih.gov/pubmed/21281505
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/bcr2822
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