Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder

作者:Newbury Dianne F*; Mari Francesca; Akha Elham Sadighi; MacDermot Kay D; Canitano Roberto; Monaco Anthony P; Taylor Jenny C; Renieri Alessandra; Fisher Simon E; Knight Samantha J L
来源:European Journal of Human Genetics, 2013, 21(4): 361-365.
DOI:10.1038/ejhg.2012.166