Heterozygous Mutations in PMS2 Cause Hereditary Nonpolyposis Colorectal Carcinoma (Lynch Syndrome) von Hendriks, Yvonne M.C., Jagmohan–Changur, Shantie, van der Klift, Heleen M., Morreau, Hans, van Puijenbroek, Marjo, Tops, Carli, van Os, Theo, Wagner, Anja, Ausems, Margreet G.F.M., Gomez, Encarna, Breuning, Martijn H., Bröcker–Vriends, Annette H.J.T., Vasen, Hans F.A., Wijnen, Juul Th

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Molecular Analysis of Hereditary Nonpolyposis Colorectal Cancer in the United States: High Mutation Detection Rate among Clinically Selected Families and Characterization of an Ame... von Wagner, Anja, Barrows, Alicia, Wijnen, Juul Th, van der Klift, Heleen, Franken, Patrick F., Verkuijlen, Paul, Nakagawa, Hidewaki, Geugien, Marjan, Jaghmohan-Changur, Shantie, Breukel, Cor, Meijers-Heijboer, Hanne, Morreau, Hans, van Puijenbroek, Marjo, Burn, John, Coronel, Stephany, Kinarski, Yulia, Okimoto, Ross, Watson, Patrice, Lynch, Jane F., de la Chapelle, Albert, Lynch, Henry T., Fodde, Riccardo

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Introduction to molecular and clinical genetics of colorectal cancer syndromes von Tops, Carli M.J., PhD, Wijnen, Juul Th., PhD, Hes, Frederik J., MD, PhD

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Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance von Hendriks, Yvonne M.C., Wagner, Anja, Morreau, Hans, Menko, Fred, Stormorken, Astrid, Quehenberger, Franz, Sandkuijl, Lodewijk, Møller, Pal, Genuardi, Maurizio, van Houwelingen, Hans, Tops, Carli, van Puijenbroek, Marjo, Verkuijlen, Paul, Kenter, Gemma, van Mil, Anneke, Meijers-Heijboer, Hanne, Tan, Gita B., Breuning, Martijn H., Fodde, Riccardo, Winjen, Jull Th, Bröcker-Vriends, Annette H.J.T., Vasen, Hans

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Diagnostic Approach and Management of Lynch Syndrome (Hereditary Nonpolyposis Colorectal Carcinoma): A Guide for Clinicians von Hendriks, Yvonne M.C, de Jong, Andrea E, Morreau, Hans, Tops, Carli M.J, Vasen, Hans F, Wijnen, Juul Th, Breuning, Martijn H, Brocker-Vriends, Annette H.J.T

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Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas von van Puijenbroek, Marjo, Middeldorp, Anneke, Tops, Carli M. J., van Eijk, Ronald, van der Klift, Heleen M., Vasen, Hans F. A., Wijnen, Juul Th, Hes, Frederik J., Oosting, Jan, van Wezel, Tom, Morreau, Hans

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Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients von de Leeuw, Wiljo J. F., Dierssen, JanWillem, Vasen, Hans F. A., Wijnen, Juul Th, Kenter, Gemma G., Meijers-Heijboer, Hanne, Brocker-Vriends, Annette, Stormorken, Astrid, Moller, Pal, Menko, Fred, Cornelisse, Cees J., Morreau, Hans

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Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures von Wagner, Anja, van Kessel, Ingrid, Kriege, Mieke G, Tops, Carli M J, Wijnen, Juul Th, Vasen, Hans F A, van der Meer, Conny A, van Oostrom, Iris I H, Meijers-Heijboer, Hanne

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Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas von van Puijenbroek, Marjo, Middeldorp, Anneke, Tops, Carli M. J., van Eijk, Ronald, van der Klift, Heleen M., Vasen, Hans F. A., Wijnen, Juul Th, Hes, Frederik J., Oosting, Jan, van Wezel, Tom, Morreau, Hans

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Suspected hereditary nonpolyposis colorectal cancer : International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer (ICG-HNPCC) criteria and results of genetic dia... von PARK, J.-G, VASEN, H. F. A, WIJNEN, J. T, BABA, S, LYNCH, H. T, KYU JOO PARK, PELTOMAKI, P, PONZ DE LEON, M, RODRIGUEZ-BIGAS, M. A, LUBINSKI, J, BECK, N. E, BISGAARD, M.-L, MIYAKI, M

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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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Bias in detection of instability of the (C)8 mononucleotide repeat of MSH6 in tumours from HNPCC patients von DE LEEUW, Wiljo J. F, VAN PUIJENBROEK, Marjo, MERX, Renee, WIJNEN, Juul Th, BRÖCKER-VRIENDS, Annette H. J. T, TOPS, Carli, VASEN, Hans, CORNELISSE, Cees J, MORREAU, Hans

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Microsatellite instability (MSI) and immunohistochemical analysis of endometrial cancers as a tool to identify family members at risk for hereditary nonpolyposis colorectal cancer... von Vasen, Hans F., Leeuw, Wiljo J., Diersen, Jan-Willem, Wijnen, Juul Th, Kenter, Gemma G., Morreau, Hans

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Colonoscopic screening of carriers of mismatch repair gene mutations: Results from the dutch HNPCC registry von Vasen, Hans F., Wijnen, Juul Th, Nagengast, Fokko N., Griffioen, Gerrit G., Menko, Fred H., Taal, Babs G., Fodde, Riccardo, Kleibeuker, Jan

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An update of cancer risk in HNPCC: A study of 101 families including 58 families associated with mismatch repair mutations von Vasen, Hans F., Stormorken, Astrid, Nagengast, Fokko N., Kleibeuker, Jan, Griffioen, Gerrit G., Menko, Fred H., Fodde, Riccardo, Taal, Babs G., Moller, Pal, Th Wijnen, Juul

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Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in dutch families von van Haeringen, Arie, Bergman, Wilma, Nelen, Marcel R., van der Kooij-Meijs, Ellien, Hendrikse, Iems, Wijnen, Juul Th, Khan, Paul Meera, Klasen, Eduard C., Frants, Rune R.

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Molecular analysis of theAPC 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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Endometrial Cancer in Four Sisters: Report of a Kindred with Presumed Cancer Family Syndrome von Menko, Fred H., Verheijen, René H.M., Everhardt, Ellen, Louwé, Leoni A., Wijnen, Juul Th, Band, Sylvia C., Felt-Bersma, Richelle J.F., Vasen, Hans F.A., Khan, P.Meera

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Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk von McGuffog, Lesley, Lee, Andrew J, Kuchenbaecker, Karoline, Gaudet, Mia M, Kosel, Matthew L, Healey, Sue C, Bacot, François, Jakubowska, Anna, Schmutzler, Rita Katharina, Piedmonte, Marion R, Singer, Christian Fridolin, Friedman, Eitan A, Neuhausen, Susan L, Greene, Mark H, Andrulis, Irene L. L, Godwin, Andrew K, Yannoukakos, Drakoulis, Caldes, Trinidad, Osorio, Ana, Terry, Mary Beth Eth, Daly, Mary Beryl, van Rensburg, Elizabeth J, Tung, Nadine M, Claes, Kathleen B. M, Imyanitov, Evgeny N, Kwong, Ava, Balmaña Gelpí, Judith, Arun, Banu K, Teo, Soo, Campbell, Ian, Seynaeve, Caroline M, Ligtenberg, Marjolijn J. L, Rookus, Matti A, Devilee, Peter P, Verhoef, Senno, van Os, Theo A. M, Fineberg, Elena, Eccles, Diana M, Cook, Jacqueline A, Donaldson, Alan, Rogers, Mark T, McCann, Emma, Berthet, Pascaline, Delnatte, Capucine, Prieur, Fabienne, Sobol, H, Coupier, I, Gauthier-Villars, M, Léoné, M, Mazoyer, S, Złowocka-Perłowska, E, Lubinski, J, Ottini, L, Papi, L, Gehrig, A, Niederacher, D, Ditsch, N, Preisler-Adams, S, Varon-Mateeva, R, Wappenschmidt, B, Weber, B.H.F, Arver, B, Stenmark-Askmalm, M, Rosenquist, R, Einbeigi, Z, Nathanson, K.L, Rebbeck, T.R, Rodriguez, G.C, Friedlander, M, Bae-Jump, V.L, Lindor, N.M, Kaufman, B, Laitman, Y, Pedersen, I.S, Jensen, U.B, Sarrel, K, Mulligan, A.M, Glendon, G, Ozcelik, H, Andersen, M.K, Ding, Y.C, Teule, Alex, Lazaro Garcia, Conxi, Brunet, Joan, Pujana, Miquel Ángel, Loud, J.T, Walsh, C, Herzog, J, Tognazzo, S, Agata, S, Weaver, J, Aittomäki, K, Muranen, T.A, Miron, A, Benitez, J, Senter, L, Huo, D, Hart, S, Easton, D.F, Chenevix-Trench, G

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Immunohistochemical localization of adenosine deaminase complexing protein in intestinal mucosa and in colorectal adenocarcinoma as a marker for tumour cell heterogeneity von TEN KATE, J, WIJNEN, J. T, BOLDEWIJN, J, KHAN, P. M, BOSMAN, F. T

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