SomaticAPCmosaicism: a frequent cause of familial adenomatous polyposis (FAP)-Reference-Cited by-同舟云学术

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SomaticAPCmosaicism: a frequent cause of familial adenomatous polyposis (FAP)

Published:2007-10 Issue:10 Volume:28 Page:985-992
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Aretz Stefan,Stienen Dietlinde,Friedrichs Nicolaus,Stemmler Susanne,Uhlhaas Siegfried,Rahner Nils,Propping Peter,Friedl Waltraut

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference52 articles.

1. Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis;Aretz;Eur J Hum Genet,2004

2. Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis;Aretz;J Med Genet,2005

3. MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype;Aretz;Int J Cancer,2006

4. Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis;Bertario;J Clin Oncol,2003

5. Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate;Bisgaard;Hum Mutat,1994

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1. SMAD4 mosaicism in juvenile polyposis: Essential contribution of somatic analysis in diagnosis;American Journal of Medical Genetics Part A;2024-05-02

2. Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revision;British Journal of Surgery;2024-05

3. Use of multi-gene panels in patients at high risk of hereditary digestive cancer: Position statement of AEG, SEOM, AEGH and IMPaCT-GENÓMICA consortium;Gastroenterología y Hepatología (English Edition);2024-03

4. Revisiting the Prognostic Impact of Family History in Colorectal Cancer by Retrospective Propensity Score Matching;Anticancer Research;2023-11

5. Detection of Mosaic Sequence Variants Associated with Human Genetic Diseases;Laboratory Medicine Online;2023-10-01

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