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scopus: 6507392334

Hendriks, Y.

( Y. Hendriks)


mutation cancer family charge syndrome mutyh hnpcc patient charge msh 6 germline colorectal carrier syndrome analysis carcinoma msh 6 mutation 165cy tumours nonpolyposis colorectal cancer chd 7 gene phenotype colorectal cancer tumour endometrial colon identi fied table genet tyr 165cys microsatellite instability repair instability microsatellite endometrial cancer p.gly genetic cell carcinoma mismatch mother msh 2 brother kras 2 adenoma parent mosaicism netherland article breast chd 7 identi nonpolyposi 382asp 6322 g genetics part defect missense mutation g >t transversions department c .1784del t expression staining mlh 1 american journal jongman germline mosaicism onset category polyposi ureter chd 7 mutation mutation analysis charge association choanal atresia p.gly 12cys vasen feature p.tyr coloboma status university




3 Most Recent Publications

Familial CHARGE syndrome and the CHD7 gene: A recurrent missense mutation, intrafamilial recurrence and variability (Article)
Jongmans, M. Hoefsloot, L.H. Ravenswaaij-Arts, C.M.A. van Donk, K.P. van der Admiraal, R.J. Magee, A. Laar, I.M.B.H. van de Hendriks, Y. Verheij, J.B. Walpole, I. Brunner, H,
2008-01-01
The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family (Article)
Puijenbroek, M. van Nielsen, M. Hes, F.J. Morreau, H. Reinards, T.H.C.M. Weiss, M.M. Wagner, A. Hendriks, Y. Vasen, H. Tops, C. Wijnen, J.T. Wezel, T. van
2007-03-01
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree (Article)
Wagner, A. Krimpen, C. van Breuning, M.H. Meer, C. van der Vasen, H.F. Niermeijer, M.F. Lindhout, D. Hendriks, Y. Meijers-Heijboer, E.J. Wijnen, J. Leeuw, W.J. de Morreau, H. Hofstra, R. Tops, C. Cornelisse, C.J. Zwinderman, A.H. Bik, E. Brocker-Vriends, A.H. Fodde, R.
2001-01-01