Steinman, Kyle J <br/><br/>
16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.  [electronic resource] 

 -  American journal of medical genetics. Part A  11 2016 
 - 2943-2955 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.37820  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosome Disorders--diagnosis<br/>Chromosome Duplication<br/>Chromosomes, Human, Pair 16<br/>Cohort Studies<br/>Electroencephalography<br/>Epilepsy--diagnosis<br/>Female<br/>Genotype<br/>Humans<br/>Infant<br/>Male<br/>Middle Aged<br/>Phenotype<br/>Young Adult