Cocchella, Alessandro <br/><br/>
The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairment.  [electronic resource] 

 -  American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics  Oct 2010 
 - 1342-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-485X 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.b.31107  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Basic Helix-Loop-Helix Transcription Factors--genetics<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 2<br/>Cyclic Nucleotide Phosphodiesterases, Type 1--genetics<br/>Female<br/>Genetic Association Studies<br/>Humans<br/>Intellectual Disability--genetics<br/>Kruppel-Like Transcription Factors--genetics<br/>Speech Disorders--genetics