Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis von HEINIMANN, Karl, THOMPSON, Annick, MÜLLER, Hansjakob, FOERNZLER, Dorothee, DOBBIE, Zuzana, LOCHER, Andreas, FURIANETTO, Tamara, BADER, Eva, WOLF, Angela, MEIER, Remy, WALTER, Klaus, BAUERFEIND, Peter, MARRA, Giancarlo

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Zur Genetik der nichtalkoholischen Fettlebererkrankungen von Müller, Hansjakob, Meier, Rémy

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Aspects génétiques des stéatoses hépatiques non alcooliques von Müller, Hansjakob, Meier, Rémy

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N-acetyltransferase 2 influences cancer prevalence in hMLH1/hMSH2 mutation carriers von HEINIMANN, K, SCOTT, R. J, CHAPPUIS, P, WEBER, W, MÜLLER, H, DOBBIE, Z, HUTTER, P

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Keine molekulargenetische Untersuchung ohne genetische Beratung von Müller, Hansjakob

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Keine molekulargenetische Untersuchung ohne genetische Beratung von Müller, Hansjakob

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Identification of a modifier gene locus on chromosome 1p35-36 in familial adenomatous polyposis von DOBBIE, Z, HEINIMANN, K, BISHOP, D. T, MÜLLER, H, SCOTT, R. J

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Session 9 S29. Genetic background of risk selection for chemoprevention studies and interventions in colorectal cancer von Müller, Hansjakob

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Microsatellite Instability in Colorectal Cancer von Ponz de Leon, Maurizio, Roncucci, Luca, Heinimann, Karl, Müller, Hansjakob, Dobbie, Zuzana, Gryfe, Robert, Redston, Mark, Gallinger, Steven

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Abstract 3802: EWSR1: Identification and functional characterization of a novel target gene locus in Lynch syndrome von Piscuoglio, Salvatore, Kovac, Michal, Kishore, Shivendra, Mele, Valentina, Zavolan, Mihaela, Müller, Hansjakob, Terracciano, Luigi M., Heinimann, Karl

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Strictly defined familial male breast cancer von Güth, Uwe, Müller, Dieter, Huang, Dorothy Jane, Obermann, Ellen, Müller, Hansjakob

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Concordant colon tumors in monozygotic twins previously treated for prostate cancer von Templeton, Arnoud, Marra, Giancarlo, Valtorta, Emanuele, Heinimann, Karl, Müller, Hansjakob, Köberle, Dieter, Gillessen, Silke

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Oculopharyngeal muscular dystrophy - an under-diagnosed disorder? von Rüegg, Stephan, Lehky Hagen, Monique, Hohl, Ursula, Kappos, Ludwig, Fuhr, Peter, Plasilov, Martina, Müller, Hansjakob, Heinimann, Karl

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Novel germline CDH1 mutations in hereditary diffuse gastric cancer families von Humar, Bostjan, Toro, Tumi, Graziano, Francesco, Müller, Hansjakob, Dobbie, Zuzana, Kwang-Yang, Han, Eng, Charis, Hampel, Heather, Gilbert, Dale, Winship, Ingrid, Parry, Susan, Ward, Robyn, Findlay, Mike, Christian, Alice, Tucker, Monica, Tucker, Kathy, Merriman, Tony, Guilford, Parry

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A de Novo PABPN1 Germline Mutation in a Patient with Oculopharyngeal Muscular Dystrophy von Gürtler, Nicolas, Plasilova, Martina, Podvinec, Mihael, Boesch, Nemya, Müller, Hansjakob, Heinimann, Karl

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Germline alterations in the cyclooxygenase‐2 gene are not associated with the development of extracolonic manifestations in a large Swiss familial adenomatous polyposis kindred von Humar, Bostjan, Giovanoli, Olivier, Wolf, Angela, Attenhofer, Michéle, Bendik, Igor, Meier, Rémy, Müller, Hansjakob, Dobbie, Zuzana

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Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer von Heinimann, Karl, Scott, Rodney J., Buerstedde, Jean‐Marie, Weber, Walter, Siebold, Karl, Attenhofer, Michèle, Müller, Hansjakob, Dobbie, Zuzana

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Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC gene von Dobbie, Z, Spycher, M, Mary, J L, Häner, M, Guldenschuh, I, Hürliman, R, Amman, R, Roth, J, Müller, H, Scott, R J

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Germline mutations in the β-catenin gene are not associated with the FAP phenotype without an APC mutation von DOBBIE, ZUZANA, MÜLLER, HANSJAKOB

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Genetische Abklärungen bei Verdacht auf das Vorliegen von Veranlagung für Tumorkrankheiten, speziell für Kolorektalkarzinome von Müller, Hj

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