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Disambiguation of "Schmiegel, Wolff"

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No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients

, , , , , , , , , , , , and . European journal of human genetics : EJHG, 16 (5): 587–592 (2008)

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Wolff Schmiegel

Wolff-Helmut Schmiegel

Andreas Schmiegel

Dorothee Schmiegel

Armin Schmiegel

 

Other publications of authors with the same name

HNPCC-associated small bowel cancer: clinical and molecular characteristics, , , , , , , , , and 8 other author(s). Gastroenterology, 128 (3): 590–599 (2005)Risks of less common cancers in proven mutation carriers with lynch syndrome, , , , , , , , , and 14 other author(s). Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 30 (35): 4409–4415 (2012)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)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)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)Detection of Novel Biomarkers of Liver Cirrhosis by Proteomic Analysis., , , , , , , , , and 7 other author(s). Hepatology (Baltimore, Md.), 49 (4): 1257--1266 (April 2009)Immunoscreening of the Extracellular Proteome of Colorectal Cancer Cells., , , , , , , , , and . BMC cancer, (February 2010)Uncoupled Responses of Smad4-deficient Cancer Cells to TNFalpha Result in Secretion of Monomeric Laminin-Gamma2., , , , , , , , , and . Molecular cancer, 9 (1): 65 (March 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)