Striano, Pasquale <br/><br/>
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.  [electronic resource] 

 -  Archives of neurology  Mar 2012 
 - 322-30 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1538-3687 
<br/><br/><label>Standard No.: </label>10.1001/archneurol.2011.1999  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Aged<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>Computational Biology<br/>Diagnostic and Statistical Manual of Mental Disorders<br/>Epilepsy--genetics<br/>Female<br/>Gene Deletion<br/>Gene Dosage<br/>Gene Duplication<br/>Gene Rearrangement<br/>Genome-Wide Association Study<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Intellectual Disability--epidemiology<br/>Italy--epidemiology<br/>Magnetic Resonance Imaging<br/>Male<br/>Microarray Analysis<br/>Middle Aged<br/>Nervous System Diseases--epidemiology<br/>Nucleic Acid Hybridization<br/>Polymerase Chain Reaction<br/>Prospective Studies<br/>Young Adult