Clinical utility gene card for: Familial adenomatous polyposis (FAP) and attenuated FAP (AFAP)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/ejhg20117.pdf
Reference11 articles.
1. Galiatsatos P, Foulkes WD : Familial adenomatous polyposis. Am J Gastroenterol 2006; 101: 385–398.
2. Knudsen AL, Bisgaard ML, Bulow S : Attenuated familial adenomatous polyposis (AFAP). A review of the literature. Fam Cancer 2003; 2: 43–55.
3. Lagarde A, Rouelau E, Ferrari A et al: Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-years medical genetics service to French FAP patients. J Med Genet 2010; 47: 721–722.
4. Friedl W, Aretz S : Familial adenomatous polyposis: experience from a study of 1164 unrelated German polyposis patients. Hereditary Cancer Clin Pract 2005; 3: 95–114.
5. Bisgaard ML, Fenger K, Bulow S, Niebuhr E, Mohr J : Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate. Hum Mutat 1994; 3: 121–125.
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