Mignon-Ravix, Cécile <br/><br/>
Intragenic rearrangements in X-linked intellectual deficiency: results of a-CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes.  [electronic resource] 

 -  American journal of medical genetics. Part A  Aug 2014 
 - 1991-7 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.36602  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Chromosome Mapping<br/>Chromosomes, Human, X<br/>Comparative Genomic Hybridization<br/>DNA Copy Number Variations<br/>Gene Deletion<br/>Genes, X-Linked<br/>Genetic Loci<br/>Genome-Wide Association Study<br/>Humans<br/>Intellectual Disability--diagnosis<br/>Male<br/>Microfilament Proteins--genetics<br/>TRPC Cation Channels--genetics<br/>Translocation, Genetic<br/>X Chromosome Inactivation