Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas.
Clear-cut inherited Mendelian traits, such as familial adenomatous polyposis or hereditary nonpolyposis colorectal cancer, account for <4% of colorectal cancers. Another 20% of all colorectal cancers are thought to occur in individuals with a significant inherited multifactorial susceptibilit...
Päätekijät: | Fearnhead, N, Wilding, J, Winney, B, Tonks, S, Bartlett, S, Bicknell, D, Tomlinson, I, Mortensen, N, Bodmer, W |
---|---|
Aineistotyyppi: | Journal article |
Kieli: | English |
Julkaistu: |
2004
|
Samankaltaisia teoksia
-
Rare variant hypothesis for multifactorial inheritance: susceptibility to colorectal adenomas as a model.
Tekijä: Fearnhead, N, et al.
Julkaistu: (2005) -
Common and rare variants in multifactorial susceptibility to common diseases.
Tekijä: Bodmer, W, et al.
Julkaistu: (2008) -
Cyclin D1 rare variants in UK multiple adenoma and early-onset colorectal cancer patients.
Tekijä: Bonilla, C, et al.
Julkaistu: (2011) -
Cyclin D1 rare variants in UK multiple adenoma and early-onset colorectal cancer patients
Tekijä: Bonilla, C, et al.
Julkaistu: (2015) -
Genetics of colorectal cancer: hereditary aspects and overview of colorectal tumorigenesis.
Tekijä: Fearnhead, N, et al.
Julkaistu: (2002)