Nava, Caroline <br/><br/>
Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders.  [electronic resource] 

 -  European journal of human genetics : EJHG  Jan 2014 
 - 71-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2013.88  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child Development Disorders, Pervasive--etiology<br/>Child, Preschool<br/>Chromosomes, Human, Pair 15--genetics<br/>Chromosomes, Human, Pair 5--genetics<br/>Comparative Genomic Hybridization<br/>Cri-du-Chat Syndrome--genetics<br/>DNA Copy Number Variations--genetics<br/>DNA Methylation--genetics<br/>Female<br/>Genetic Association Studies<br/>Genotype<br/>Humans<br/>Infant<br/>Male<br/>Oligonucleotide Array Sequence Analysis--methods<br/>Polymorphism, Single Nucleotide--genetics<br/>Trisomy--genetics