Newbury, Dianne F <br/><br/>
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 
<br/><br/> Publication Type: Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Comment 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2012.166  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Apraxias--genetics<br/>Chromosomes, Human, Pair 16--genetics<br/>Humans<br/>Sequence Deletion