Yamamoto, Toshiyuki <br/><br/>
Overlapping microdeletions involving 15q22.2 narrow the critical region for intellectual disability to NARG2 and RORA.  [electronic resource] 

 -  European journal of medical genetics  Mar 2014 
 - 163-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2014.02.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child, Preschool<br/>Chromosome Banding<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 15--genetics<br/>DNA Copy Number Variations<br/>Female<br/>Genetic Association Studies--methods<br/>Genotype<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Intellectual Disability--genetics<br/>Male<br/>Nuclear Proteins--genetics<br/>Nuclear Receptor Subfamily 1, Group F, Member 1--genetics<br/>Phenotype<br/>Transcriptional Elongation Factors<br/>Young Adult