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 DF; Mari F; Sadighi Akha E; Macdermot KD; Canitano R; Monaco AP; Taylor JC; Renieri A; Fisher SE; Knight SJPublicationEuropean journal of human genetics : EJHG, 2013, Vol 21, Issue 4, p361ISSN1476-5438Publication typearticleDOI10.1038/ejhg.2012.166