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pro vyhledávání: '"Michelle W Condie"'
Autor:
Randall W. Burt, Angela L. Schwab, Deborah W. Neklason, Thérèse M. F. Tuohy, Michelle W Condie
Publikováno v:
Familial Cancer. 7:173-177
De novo mutations in the adenomatous polyposis coli (APC) gene are estimated to constitute approximately 25% of familial adenomatous polyposis (FAP) cases. A small percentage of these arise in the mosaic form, affecting only a subset of cells in the
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 8, Iss Suppl 1, p O1 (2010)
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice
Background Familial adenomatous polyposis (FAP) is a colon cancer syndrome with a prevalence of 1:10:000, hallmarked by 100s to 1000s of precancerous colonic polyps and nearly 100% lifetime risk of developing colon cancer at an average age of 39 year