Figure 2From: Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2Skull and skeletal abnormalities in two subjects. a, b) brachycephaly in Subject 1 (a) and 2 (b); c) occipital asymmetry in Subject 1; d) congenital C1-C2 vertebral block; e) accentuation of dorsal kiphosis (arrow) in subject 2.Back to article page