Gazou, Anastasia <br/><br/>
Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disability.  [electronic resource] 

 -  American journal of medical genetics. Part A  Apr 2013 
 - 860-4 p.  digital 
<br/><br/> Publication Type: Case Reports; 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.35778  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Human, X<br/>Coenzyme A Ligases--genetics<br/>Facies<br/>Gene Deletion<br/>Genome-Wide Association Study<br/>Genotype<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Intellectual Disability--genetics<br/>Male<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>Long-Chain-Fatty-Acid-CoA Ligase