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

Weemaes, C.M.R.; Tol, M.J.D. van; Wang, J.; Ostaijen-ten Dam, M.M. van; Eggermond, M.C.J.A. van; Thijssen, P.E.; ... ; Maarel, S.M. van der (2013)

Article / Letter to editor

• ICF syndrome
• DNMT3B
• ZBTB24
• genotype-phenotype

• All authors: Weemaes, C.M.R.; Tol, M.J.D. van; 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; Maarel, S.M. van der
• Date: 2013-11-30
• Journal: European Journal of Human Genetics
• Volume: 21
• Issue: 11
• Pages: 1219 - 1225
• DOI: doi:10.1038/ejhg.2013.40