Afdeling/polikliniek
afdeling Genetica
Publicaties
- Van der Klift, HM, Mensenkamp, AR, Drost, M, Bik, EC, Vos, YJ , Gille, HJJP, Redeker, BEJW, Tiersma, Y, Zonneveld, JBM, García, EG, Letteboer, TGW, Olderode-Berends, MJW, van Hest, LP, van Os, TA, Verhoef, S, Wagner, A, van Asperen, CJ, Ten Broeke, SW, Hes, FJ, de Wind, N, Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency (CMMRD) Syndrome 20 Jul 2016 Human Mutation.
- Jansen, AM, van Wezel, T, van den Akker, BE, Ventayol Garcia, M, Ruano, D, Tops, CM, Wagner, A, Letteboer, TG, Gómez-García, EB, Devilee, P, Wijnen, JT, Hes, FJ & Morreau, H. Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancers, Jul 2016 European Journal of Human Genetics. 24, 7,1089-92.
- Ghorbanoghli, Z, Nieuwenhuis MH, Houwing-Duistermaat, JJ, Jagmohan-Changur, S, Hes, FJ, Tops, CM, Wagner, A, Aalfs, CM, Verhoef, S, Gómez García, EB, Sijmons, RH, Menko, FH, Letteboer, TG, Hoogerbrugge, N, van Wezel, T, Vasen, HFA & Wijnen, JT. Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers. 15 Feb 2016 Familial Cancer. p. 1-8.
Deze en meer publicaties van dr. TGW Letteboer zijn te raadplegen via PubMed.