Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer

INTRODUCTION: Mutations in known predisposition genes account for only about a third of all multiple-case breast cancer families. We hypothesized that germline mutations in FANCD2, BRIP1/BACH1, LMO4 and SFN may account for some of the unexplained multiple-case breast cancer families. METHODS: The fa...

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Bibliografiska uppgifter
Huvudupphovsmän: Lewis, Aaron G, Flanagan, James, Marsh, Anna, Pupo, Gulietta M, Mann, Graham, Spurdle, Amanda B, Lindeman, Geoffrey J, Visvader, Jane E, Brown, Melissa A, Chenevix-Trench, Georgia
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2005
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1410737/
https://ncbi.nlm.nih.gov/pubmed/16280053
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/bcr1336
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