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Gut|April 16, 2005
The C/C-13910 genotype of adult-type hypolactasia is associated with an increased risk of colorectal cancer in the Finnish populationH Rasinperä, C Forsblom, N S Enattah, et al.Cancer Research|March 14, 2001
MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancerJ Huang, S A Kuismanen, T Liu, et al.British Journal of Cancer|November 8, 2012
Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancerK Kämpjärvi, N Mäkinen, O Kilpivaara, et al.British Journal of Cancer|August 14, 2014
Identification of 33 candidate oncogenes by screening for base-specific mutationsS Tuupanen, U A Hänninen, J Kondelin, et al.Journal of Medical Genetics|March 1, 2007
Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)H F A Vasen, G Möslein, A Alonso, et al.British Journal of Cancer|June 16, 2005
Gene expression signatures for colorectal cancer microsatellite status and HNPCCM Kruhøffer, J L Jensen, P Laiho, et al.American Journal of Human Genetics|September 6, 2001
Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromesX P Zhou, K Woodford-Richens, R Lehtonen, et al.Gut|January 16, 2008
Guidelines for the clinical management of familial adenomatous polyposis (FAP)H F A Vasen, G Möslein, A Alonso, et al.Gut|June 29, 2010
Peutz-Jeghers syndrome: a systematic review and recommendations for managementA D Beggs, A R Latchford, H F A Vasen, et al.Familial Cancer|September 19, 2009
Recommendations to improve identification of hereditary and familial colorectal cancer in EuropeH F A Vasen, G Möslein, A Alonso, et al.Pageof 10