We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleDual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.AuthorsNewbury, Dianne F; Mari, Francesca; Sadighi Akha, Elham; Macdermot, Kay D; Canitano, Roberto; Monaco, Anthony P; Taylor, Jenny C; Renieri, Alessandra; Fisher, Simon E; Knight, Samantha J LPublicationEuropean journal of human genetics : EJHG, 2013, Vol 21, Issue 4, p361ISSN1476-5438Publication typeResearchDOI10.1038/ejhg.2012.166