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Disambiguation of "Propping, Peter"

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Expanded extracolonic tumor spectrum in MUTYH-associated polyposis

, , , , , , , , , , , and . Gastroenterology, 137 (6): 1976-85.e1-10 (2009)

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Peter Propping

Ernst Propping

Dirk Propping

Stefan Propping

Walter Propping

 

Other publications of authors with the same name

Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study, , , , , , , , , and 12 other author(s). BMC gastroenterology, (2010)Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer, , , , , , , , , and 10 other author(s). International journal of cancer. Journal international du cancer, 116 (5): 692–702 (2005)No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients, , , , , , , , , and 3 other author(s). European journal of human genetics : EJHG, 16 (5): 587–592 (2008)Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer, , , , , , , , , and 9 other author(s). Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 8 (2): 174–182 (2010)Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin, , , , , , , , , and 14 other author(s). PloS one, 6 (6): e20464 (2011)Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications, , , , , , , , , and 19 other author(s). International journal of molecular epidemiology and genetics, 2 (1): 36–50 (2011)Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility, , , , , , , , , and 24 other author(s). Carcinogenesis, 31 (9): 1612–1619 (2010)Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3, , , , , , , , , and 16 other author(s). Carcinogenesis, 35 (2): 315–323 (2014)Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome, , , , , and . Deutsches Ärzteblatt international, 110 (3): 32–38 (2013)Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium, , , , , , , , , and 10 other author(s). Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 24 (26): 4285–4292 (2006)