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

Newbury, Dianne F

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. [electronic resource] - European journal of human genetics : EJHG Apr 2013 - 361-5 p. digital

Publication Type: Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Comment

1476-5438

10.1038/ejhg.2012.166 doi


Apraxias--genetics
Chromosomes, Human, Pair 16--genetics
Humans
Sequence Deletion