Tsuchida, N <br/><br/>
Detection of copy number variations in epilepsy using exome data.  [electronic resource] 

 -  Clinical genetics  03 2018 
 - 577-587 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.13144  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Alleles<br/>Child<br/>Child, Preschool<br/>Comparative Genomic Hybridization<br/>Computational Biology--methods<br/>DNA Copy Number Variations<br/>Epilepsy--diagnosis<br/>Exome<br/>Female<br/>Genetic Association Studies--methods<br/>Genetic Predisposition to Disease<br/>Genetic Testing--methods<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Exome Sequencing<br/>Young Adult