Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects

Author(s):
Weemaes, C.M.R.; Tol, M.J.D. van (0000-0003-1600-4279); Wang, J.; Ostaijen-ten Dam, M.M. van; Eggermond, M.C.J.A. van; Thijssen, P.E.; Aytekin, C.; Brunetti-Pierri, N.; Burg, M. van der; Davies, E.G.; Ferster, A.; Furthner, D.; Gimelli, G.; Gennery, A.; Kloeckener-Gruissem, B.; Meyn, S.; Powell, C.; Reisli, I.; Schuetz, C.; Schulz, A.; Shugar, A.; Elsen, P.J. van den (0000-0002-5196-0082); Maarel, S.M. van der (0000-0001-8103-711X)
Published
2013
Publication type
Article / Letter to editor
ICF syndromeDNMT3BZBTB24genotype-phenotype
Date issued
2013-11-30
Language
English
Is part of
European Journal of Human Genetics (2013), Vol. 21, no. 11, p. 1219-1225
hdl
1887/100403
doi
10.1038/ejhg.2013.40