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(1 - 4 of 4)
Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?
Suerink, M.; Potjer, T.P.; Versluijs, A.B.; Broeke, S.W. ten; Tops, C.M.; Wimmer, K.; Nielsen, M. 2018
Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?
Article / Letter to editor
metadata only
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
Suerink, M.; Klift, H.M. van der; Broeke, S.W. ten; Dekkers, O.M.; Bernstein, I.; Munar, G.C.; ... ; Nielsen, M. 2016
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
Article / Letter to editor
open access
Germ-line variants identified by next generation sequencing in a panel of estrogen and cancer associated genes correlate with poor clinical outcome in Lynch syndrome patients
Jori, B.; Kamps, R.; Xanthoulea, S.; Delvoux, B.; Blok, M.J.; Vijver, K.K. van de; ... ; Romano, A. 2015
Germ-line variants identified by next generation sequencing in a panel of estrogen and cancer associated genes correlate with poor clinical outcome in Lynch syndrome patients
Article / Letter to editor
metadata only
Insertion of an SVA element, a nonautonomous retrotransposon, in PMS2 intron 7 as a novel cause of lynch syndrome
Klift, H.M.D. van der; Tops, C.M.; Hes, F.J.; Devilee, P.; Wijnen, J.T. 2012
Insertion of an SVA element, a nonautonomous retrotransposon, in PMS2 intron 7 as a novel cause of lynch syndrome
Article / Letter to editor
metadata only