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Clinical Genetics|March 18, 2006
A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instabilityF Marroni, C Pastrello, P Benatti, et al.International Journal of Cancer|August 9, 2001
Clinical and biologic heterogeneity of hereditary nonpolyposis colorectal cancerP Benatti, L Roncucci, D Ganazzi, et al.Gut|June 16, 1999
Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosisM P de Leon, M Pedroni, P Benatti, et al.British Journal of Cancer|February 19, 2004
Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancerM Ponz de Leon, P Benatti, C Di Gregorio, et al.Disease Markers|May 3, 2007
A mononucleotide markers panel to identify hMLH1/hMSH2 germline mutationsM Pedroni, B Roncari, S Maffei, et al.Gut|December 20, 2003
Aetiology of colorectal cancer and relevance of monogenic inheritanceM Ponz de Leon, P Benatti, F Borghi, et al.Clinical Genetics|August 28, 2007
Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCCB Roncari, M Pedroni, S Maffei, et al.Annals of the New York Academy of Sciences|November 15, 2006
SDH mutations in patients affected by paraganglioma syndromes: a personal experienceM Mannelli, L Simi, T Ercolino, et al.Community Genetics|June 5, 2004
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristicsA Viel, M Genuardi, E Lucci-Cordisco, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 2, 2001
Molecular screening for hereditary nonpolyposis colorectal cancer: a prospective, population-based studyA Percesepe, F Borghi, M Menigatti, et al.Pageof 9