Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer von Wijnen, Juul T, Vasen, Hans F.A, Khan, P. Meera, Zwinderman, Aeilko H, van der Klift, Heleen, Mulder, Adri, Tops, Carli, Møller, Pål, Fodde, Riccardo, Menko, Fred, Taal, Babs, Nagengast, Fokko, Brunner, Han, Kleibeuker, Jan, Sijmons, Rolf, Griffioen, Gerrit, Bröcker-Vriends, Annette, Bakker, Egbert, van Leeuwen-Cornelisse, Inge, Meijers-Heijboer, Anne, Lindhout, Dick, Breuning, Martijn, Post, Jan, Schaap, Cees, Apold, Jaran, Heimdal, Ketil, Bertario, Lucio, Bisgaard, Marie Luise, Goetz, Petr

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Hereditary Nonpolyposis Colorectal Cancer Families Not Complying with the Amsterdam Criteria Show Extremely Low Frequency of Mismatch-Repair-Gene Mutations von Wijnen, Juul, Khan, P. Meera, Vasen, Hans, van der Klift, Heleen, Mulder, Adri, van Leeuwen-Cornelisse, Inge, Bakker, Bert, Losekoot, Monique, Møller, Pål, Fodde, Riccardo

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Molecular genetic tests as a guide to surgical management of familial adenomatous polyposis von Vasen, HFA, van der Luijt, RB, Slors, JFM, Buskens, E, de Ruiter, P, Baeten, CGM, Schouten, WR, Oostvogel, HJM, Kuijpers, JHC, Tops, CMJ, Khan, P Meera

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Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli von van der Luijt, R B, Meera Khan, P, Vasen, H F, Breukel, C, Tops, C M, Scott, R J, Fodde, R

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Apc1638T: a mouse model delineating critical domains of the adenomatous polyposis coli protein involved in tumorigenesis and development von Smits, R, Kielman, M F, Breukel, C, Zurcher, C, Neufeld, K, Jagmohan-Changur, S, Hofland, N, van Dijk, J, White, R, Edelmann, W, Kucherlapati, R, Khan, P M, Fodde, R

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The international collaborative group on hereditary non-polyposis colorectal cancer (ICG-HNPCC) von VASEN, H. F. A, MECKLIN, J.-P, KHAN, P. M, LYNCH, H. T

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Surveillance in hereditary nonpolyposis colorectal cancer : an international cooperative study of 165 families von VASEN, H. F, MECKLIN, J.-P, LYNCH, H. T, WATSON, P, UTSUNOMIYA, J, BERTARIO, L, LYNCH, P, SVENDSEN, L. B, CRISTOFARO, G, MÜLLER, H, MEERA KHAN, P

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The genetic background modifies the spontaneous and X-ray-induced tumor spectrum in the Apc1638N mouse model von van der Houven van Oordt, C. Willemien, Smits, Ron, Schouten, Theo G., Houwing-Duistermaat, Jeanine J., Williamson, Sophia L.H., Luz, Arne, Khan, P. Meera, van der Eb, Alex J., Breuer, Marco L., Fodde, Riccardo

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Interval cancers in hereditary non-polyposis colorectal cancer (Lynch syndrome) von Vasen, H.F.A., Nagengast, F.M., Meera Khan, P.

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Relationship Between Patterns of Engraftment in Peripheral Blood and Immune Reconstitution After Allogeneic Bone Marrow Transplantation for (Severe) Combined Immunodeficiency von van Leeuwen, J.E.M., van Tol, M.J.D., Joosten, A.M., Schellekens, P.T.A., van den Bergh, R. Langlois, Waaijer, J.L.M., Oudeman-Gruber, N.J., van der Weijden-Ragas, C.P.M., Roos, M.T.L., Gerritsen, E.J.A., van den Berg, H., Haraldsson, A., Khan, P. Meera, Vossen, J.M.

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A cost‐effectiveness analysis of colorectal screening for hereditary nonpolyposis colorectal carcinoma gene carriers von Vasen, Hans F. A., Ballegooijen, Marjolein van, Buskens, Eric, Kleibeuker, Jan K., Taal, Babs G., Griffioen, Gerrit, Nagengast, Fokko M., Menko, Fred H., Khan, P. Meera

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Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3′ APC mutation von Kartheuser, Alex, Walon, Corinne, West, Sarah, Breukel, Cor, Detry, Roger, Gribomont, Anne-Catherine, Hamzehloei, Tayebeh, Hoang, Pierre, Maiter, Dominique, Pringot, Jacques, Rahier, Jacques, Khan, P Meera, Curtis, Ann, Burn, John, Fodde, Riccardo, Verellen-Dumoulin, Christine

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Mechanisms of APC-driven tumorigenesis: lessons from mouse models von Fodde, R., Smits, R., Hofland, N., Kielman, M., Meera Khan, P.

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Rapid Detection of Translation-Terminating Mutations at the Adenomatous Polyposis Coli (APC) Gene by Direct Protein Truncation Test von van der Luijt, Rob, Khan, P.Meera, Vasen, Hans, van Leeuwen, Claus, Tops, Carli, Roest, Pauline, den Dunnen, Johan, Fodde, Riccardo

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MSH2 genomic deletions are a frequent cause of HNPCC von Wijnen, J, van der Klift, H, Vasen, H, Khan, P M, Menko, F, Tops, C, Meijers Heijboer, H, Lindhout, D, Møller, P, Fodde, R

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Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16 von WIJNEN, J, MEERA KHAN, P, GRIFFIOEN, G, CATS, A, KLEIBEUKER, J, VARESCO, L, BERTARIO, L, BISGAARD, M.-L, MOHR, J, KOLODNER, R, FODDE, R, VASEN, H, MENKO, F, VAN DER KLIFT, H, VAN DEN BROEK, M, VAN LEEUWEN-CORNELISSE, I, NAGENGAST, F, MEIJERS-HEIJBOER, E. J, LINDHOUT, D

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Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis von van der Luijt, Rob. B., Khan, P. Meera, Vasen, Hans F. A., Tops, Carli M. J., van Leeuwen-Cornelisse, Inge S. J., Wijnen, Juul Th, van der Klift, Heleen M., Plug, Rob J., Griffioen, Gerrit, Fodde, Riccardo

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Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis von WIJNEN, J, VASEN, H, LINDHOUT, D, GRIFFIOEN, G, CATS, A, KLEIBEUKER, J, VARESCO, L, BERTARIO, L, BISGAARD, M. L, MOHR, J, FODDE, R, MEERA KHAN, P, MENKO, F. H, VAN DER KLIFT, H, VAN LEEUWEN, C, VAN DEN BROEK, M, VAN LEEUWEN-CORNELISSE, I, NAGENGAST, F, MEIJERS-HEIJBOER, A

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APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis von VAN DER LUIJT, R. B, VASEN, H. F. A, TOPS, C. M. J, BREUKEL, C, FODDE, R, MEERA KHAN, P

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Evidence for a gene on 17p13.3, distal to TP53, as a target for allele loss in breast tumors without p53 mutations von CORNELIS, R. S, VAN VLIET, M, VOS, C. B. J, CLETON-JANSEN, A.-M, VAN DE VIJVER, M. J, PETERSE, J. L, MEERA KHAN, P, BØRRESEN, A.-L, CORNELISSE, C. J, DEVILEE, P

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