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...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: 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
التنسيق: Artigo
اللغة:Inglês
منشور في: BioMed Central 2011
الموضوعات:
Research Article
الوصول للمادة أونلاين: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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