Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?

Author(s):
Suerink, M.; Potjer, T.P.; Versluijs, A.B.; Broeke, S.W. ten; Tops, C.M. (0000-0002-6769-7290); Wimmer, K.; Nielsen, M.
Published
2018
Publication type
Article / Letter to editor
bMMRDcafe-au-lait maculesCMMRDhereditary cancer syndromesHNPCCLynch syndromePMS2recessive genetic conditions
Date issued
2018-01-31
Language
English
Is part of
Clinical Genetics (2018), Vol. 93, no. 1, p. 134-137
hdl
1887/95502
doi
10.1111/cge.13053