Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome
Author(s):
Klift, H.M. van der; Mensenkamp, A.R.; Drost, M.; Bik, E.C.; Vos, Y.J.; Gille, H.J.J.P.; Redeker, B.E.J.W.; Tiersma, Y. (0000-0001-7691-654X); Zonneveld, J.B.M.; Garcia, E.G.; Letteboer, T.G.W.; Olderode-Berends, M.J.W.; Hest, L.P. van; Os, T.A. van; Verhoef, S.; Wagner, A.; Asperen, C.J. van (0000-0002-1436-7650); Broeke, S.W. ten; Hes, F.J. (0000-0002-3025-0882); Wind, N. de (0000-0002-3143-5061); Nielsen, M.; Devilee, P. (0000-0002-8023-2009); Ligtenberg, M.J.L.; Wijnen, J.T. (0000-0003-2805-6922); Tops, C.M.J.
