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Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study, , , , , , , , , und 4 andere Autor(en). The Lancet. Oncology, 6 (8): 566–572 (2005)Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium, , , , , , , , , und 10 andere Autor(en). Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 24 (26): 4285–4292 (2006)N-acetyltransferase (NAT) 2 acetylator status and age of onset in patients with hereditary nonpolyposis colorectal cancer (HNPCC), , , , , , , , , und 3 andere Autor(en). Cancer letters, 241 (1): 150–157 (2006)Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer, , , , , , , , , und 4 andere Autor(en). Cancer letters, 236 (2): 191–197 (2006)Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer, , , , , , , , , und 10 andere Autor(en). International journal of cancer. Journal international du cancer, 116 (5): 692–702 (2005)Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium, , , , , , , , , und 3 andere Autor(en). Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 22 (22): 4486–4494 (2004)HNPCC-associated small bowel cancer: clinical and molecular characteristics, , , , , , , , , und 8 andere Autor(en). Gastroenterology, 128 (3): 590–599 (2005)Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer, , , , , , , , , und 10 andere Autor(en). International journal of cancer. Journal international du cancer, 118 (1): 115–122 (2006)Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue, , , , , , , , , und 4 andere Autor(en). Human mutation, 23 (3): 285 (2004)