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Results: 1-10 |
Results: 10

Authors: Berends, MJW Wu, Y Sijmons, RH Mensink, RGJ van der Sluis, T Hordijk-Hos, JM de Vries, EGE Hollema, H Karrenbeld, A Buys, CHCM van der Zee, AGJ Hofstra, RMW Kleibeuker, JH
Citation: Mjw. Berends et al., Molecular and clinical characteristics of MSH6 variants: An analysis of 25index carriers of a germline variant, AM J HU GEN, 70(1), 2002, pp. 26-37

Authors: Wu, Y Berends, MJW Sijmons, RH Mensink, RGJ Verlind, E Kooi, KA van der Sluis, T Kempinga, C van der Zee, AGJ Hollema, H Buys, CHCM Kleibeuker, JH Hofstra, RMW
Citation: Y. Wu et al., A role for MLH3 in hereditary nonpolyposis colorectal cancer, NAT GENET, 29(2), 2001, pp. 137-138

Authors: Berends, MJW Tan-Sindhunata, G Leegte, B Van Essen, AJ
Citation: Mjw. Berends et al., Phenotypic variability of cat-eye syndrome, GEN COUNSEL, 12(1), 2001, pp. 23-34

Authors: Berends, MJW Wu, Y Sijmons, RH Hofstra, RMW van der Zee, AGJ Buys, CHCM Kleibeuker, JH
Citation: Mjw. Berends et al., Clinical definition of hereditary non-polyposis colorectal cancer: A search for the impossible?, SC J GASTR, 36, 2001, pp. 61-67

Authors: Berends, MJW Hollema, H Wu, Y van der Sluis, T Mensink, RGJ ten Hoor, KA Sijmons, RH de Vries, EGE Pras, E Mourits, MJE Hofstra, RMW Buys, CHCM Kleibeuker, JH van der Zee, AGJ
Citation: Mjw. Berends et al., MLH1 and MSH2 protein expression as a pre-screening marker in hereditary and non-hereditary endometrial hyperplasia and cancer, INT J CANC, 92(3), 2001, pp. 398-403

Authors: Wu, Y Berends, MJW Post, JG Mensink, RGJ Verlind, E Van Der Sluis, T Kempinga, C Sijmons, RH Van der Zee, AGJ Hollema, H Kleibeuker, JH Buys, CHCM Hofstra, RMW
Citation: Y. Wu et al., Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms, GASTROENTY, 120(7), 2001, pp. 1580-1587

Authors: Berends, MJW Cats, A Hollema, H Karrenbeld, A Beentjes, JAM Sijmons, RH Mensink, RGJ Hofstra, RMW Verschueren, RCJ Kleibeuker, JH
Citation: Mjw. Berends et al., Adrenocortical adenocarcinoma in an MSH2 carrier: Coincidence or causal relation?, HUMAN PATH, 31(12), 2000, pp. 1522-1527

Authors: Berends, MJW Kleibeuker, JH de Vries, EGE Mourits, MJE Hollema, H Pras, E van der Zee, AGJ
Citation: Mjw. Berends et al., The importance of family history in young patients with endometrial cancer, EUR J OB GY, 82(2), 1999, pp. 139-141

Authors: Berends, MJW Hordijk, R Scheffer, H Oosterwijk, JC Halley, DJJ Sorgedrager, N
Citation: Mjw. Berends et al., Two cases of maternal uniparental disomy 14 with a phenotype overlapping with the Prader-Willi phenotype, AM J MED G, 84(1), 1999, pp. 76-79

Authors: Wu, Y Berends, MJW Mensink, RGJ Kempinga, C Sijmons, RH van der Zee, AGJ Hollema, H Kleibeuker, JH Buys, CHCM Hofstra, RMW
Citation: Y. Wu et al., Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations, AM J HU GEN, 65(5), 1999, pp. 1291-1298
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