Zarchi, Omer <br/><br/>
Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes.  [electronic resource] 

 -  Journal of psychiatric research  Nov 2013 
 - 1623-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1879-1379 
<br/><br/><label>Standard No.: </label>10.1016/j.jpsychires.2013.07.004  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>22q11 Deletion Syndrome--genetics<br/>Acoustic Stimulation<br/>Adolescent<br/>Adult<br/>Catechol O-Methyltransferase--genetics<br/>Child<br/>Contingent Negative Variation--genetics<br/>Endophenotypes<br/>Female<br/>Genetic Association Studies<br/>Genetic Predisposition to Disease<br/>Genotype<br/>Humans<br/>Male<br/>Polymorphism, Single Nucleotide--genetics<br/>Proline Oxidase--genetics<br/>Schizophrenia--physiopathology<br/>Sensory Gating--genetics<br/>Young Adult