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British Journal of Cancer|November 11, 2010
A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variantsE Theodoratou, H Campbell, A Tenesa, et al.American Journal of Human Genetics|November 28, 2002
The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish populationW D Foulkes, I Thiffault, S B Gruber, et al.Nature Genetics|March 1, 1996
The complete BRCA2 gene and mutations in chromosome 13q-linked kindredsS V Tavtigian, J Simard, J Rommens, et al.British Journal of Cancer|November 19, 2009
Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)A Osorio, R L Milne, G Pita, et al.Pageof 9