Hamdan, Fadi F <br/><br/>
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.  [electronic resource] 

 -  American journal of human genetics  Nov 2010 
 - 671-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2010.09.017  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Amino Acid Sequence<br/>Child<br/>Child Development Disorders, Pervasive--genetics<br/>Child, Preschool<br/>Female<br/>Forkhead Transcription Factors--genetics<br/>Humans<br/>Intellectual Disability--genetics<br/>Language Disorders--genetics<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Repressor Proteins--genetics