Ching, Michael S L <br/><br/>
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.  [electronic resource] 

 -  American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics  Jun 2010 
 - 937-47 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-485X 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.b.31063  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Autistic Disorder--genetics<br/>Child<br/>Child Development Disorders, Pervasive--genetics<br/>Comparative Genomic Hybridization<br/>Developmental Disabilities--genetics<br/>Female<br/>Humans<br/>Intellectual Disability--genetics<br/>Language Development Disorders--genetics<br/>Male<br/>Mutation<br/>Phenotype<br/>Schizophrenia--genetics<br/>Sequence Deletion