DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.

Jang, Y. L.; Rigolet, M.; Bourchis, D.; Nigon, F.; Bokesoy, I.; Fryns, J. P.; Hulten, M.; Jonveaux, P.; Maraschio, Paola; Megarbane, A.; Moncla, A.; VIEGAS PEQUIGNOT, E.