Zeesman, Susan <br/><br/>
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.  [electronic resource] 

 -  American journal of medical genetics. Part A  Mar 2006 
 - 509-14 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.31110  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Apraxias--pathology<br/>Child, Preschool<br/>Chromosome Banding<br/>Chromosome Deletion<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 7--genetics<br/>Female<br/>Forkhead Transcription Factors--genetics<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Karyotyping<br/>Language Disorders--pathology<br/>Microsatellite Repeats--genetics<br/>Speech Disorders--pathology