Interstitial 12p deletion involving more than 40 genes in a patient with postnatal microcephaly, psychomotor delay, optic nerve atrophy, and facial dysmorphism
Titel:
Interstitial 12p deletion involving more than 40 genes in a patient with postnatal microcephaly, psychomotor delay, optic nerve atrophy, and facial dysmorphism
Auteur:
Hoppe, Anne Heinemeyer, Jan Klopocki, Eva Graul-Neumann, Luitgard M. Spors, Birgit Bittigau, Petra Kaindl, Angela M.