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

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Newbury, D. ; Mari, F. ; Akha, E. ; MacDermot, K. ; Canitano, R. ; Monaco, A. ; Taylor, J. ; Renieri, A. ; Fisher, S. ; Knight, S. (2013)

In this issue, Raca et al1 present two cases of childhood apraxia of speech (CAS) arising from microdeletions of chromosome 16p11.2. They propose that comprehensive phenotypic profiling may assist in the delineation and classification of such cases. To complement this s... View more