Agha, Zehra <br/><br/>
Exome sequencing identifies three novel candidate genes implicated in intellectual disability.  [electronic resource] 

 -  PloS one  2014 
 - e112687 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0112687  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acyltransferases--genetics<br/>Adolescent<br/>Adult<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 9--genetics<br/>Craniofacial Abnormalities--genetics<br/>Exome<br/>Female<br/>Genes, Dominant<br/>Genes, Recessive<br/>Heart Defects, Congenital--genetics<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Mutation, Missense<br/>Myeloid-Lymphoid Leukemia Protein--genetics<br/>Pedigree<br/>Repressor Proteins--genetics