and skeletal anomalies. We report a clinical and molecular study of 39 patients affected by KBG syndrome. Among them, . et al. 0 19 were diagnosed after the detection of a 16q24.3 deletion encompassing the ANKRD11 gene by array CGH. In the 20 remaining patients - issue: - volume: - pages: .
, . et al. 0 Multiple congenital malformations arise from somatic mosaicism for constitutively active Pik3ca signaling - issue: - volume: - pages: .