Familiäre adenomatöse Polyposis und andere Polyposissyndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology
Link
http://link.springer.com/content/pdf/10.1007/s11377-009-0342-y.pdf
Reference23 articles.
1. Aretz S, Uhlhaas S, Goergens H, Siberg K et al (2006) MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype. Int J Cancer 119:807
2. Aretz S, Stienen D, Friedrichs N et al (2007) Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP). Hum Mutat 28: 985–992
3. Boparai KS, Dekker E, Susanne van Eeden S van et al (2008) Hyperplastic polyps and sessile serrated adenomas as a phenotypic expression of MYH-associated polyposis. Gastroenterology 135: 2014–2018
4. Carvajal-Carmona LG, Howarth KM, Lockett M et al (2007) Molecular classification and genetic pathways in hyperplastic polyposis syndrome. J Pathol 212: 378–385
5. Castells A (2008) MYH-associated polyposis and hyperplastic polyps, partners in crime? Gastroenterology 135: 1857–1859
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