Role of rare variants in undetermined multiple adenomatous polyposis and early-onset colorectal cancer
Some 15-20% of multiple adenomatous polyposis have no genetic explanation and 20-30% of colorectal cancer (CRC) cases are thought to be due to inherited multifactorial causes. Accumulation of deleterious effects of low-frequency dominant and independently acting variants may be a partial explanation...
المؤلفون الرئيسيون: | Lefevre, J, Bonilla, C, Colas, C, Winney, B, Johnstone, E, Tonks, S, Day, T, Hutnik, K, Boumertit, A, Soubrier, F, Midgley, R, Kerr, D, Parc, Y, Bodmer, W |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
Nature Publishing Group
2012
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مواد مشابهة
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Role of rare variants in undetermined multiple adenomatous polyposis and early-onset colorectal cancer.
حسب: Lefevre, J, وآخرون
منشور في: (2012) -
Cyclin D1 rare variants in UK multiple adenoma and early-onset colorectal cancer patients.
حسب: Bonilla, C, وآخرون
منشور في: (2011) -
Cyclin D1 rare variants in UK multiple adenoma and early-onset colorectal cancer patients
حسب: Bonilla, C, وآخرون
منشور في: (2015) -
Familial adenomatous polyposis (FAP) and its gene, APC.
حسب: Bodmer, W
منشور في: (1999) -
Familial adenomatous polyposis
حسب: Rozen Paul, وآخرون
منشور في: (2009-10-01)