Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay

Por Fryssira, H., Tsoutsou, E., Psoni, S., Amenta, S., Liehr, T., Anastasakis, E., Skentou, Ch, Ntouflia, A., Papoulidis, I., Manolakos, E., Chaliasos, N.
Publicado no Mol Cytogenet (2016)