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

Authors :: Newbury, D.F.
Mari, F.
Akha, E.S.
MacDermot, K.D.
Canitano, R.
Monaco, A.P.
Taylor, J.C.
Renieri, A.
Fisher, S.E.
Knight, S.J.L.
Newbury, D.F.
Mari, F.
Akha, E.S.
MacDermot, K.D.
Canitano, R.
Monaco, A.P.
Taylor, J.C.
Renieri, A.
Fisher, S.E.
Knight, S.J.L.
Source :: European Journal of Human Genetics; 361; 365; 1018-4813; 4; 21; ~European Journal of Human Genetics~361~365~~~1018-4813~4~21~~
Publication Year :: 2013
Abstract: Contains fulltext : 111324.pdf (publisher's version ) (Closed access)

Database :: OAIster
Journal :: European Journal of Human Genetics; 361; 365; 1018-4813; 4; 21; ~European Journal of Human Genetics~361~365~~~1018-4813~4~21~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1284070978
Document Type :: Electronic Resource

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