Valdes-Miranda, Juan Manuel <br/><br/>
A novel microdeletion involving the 13q31.3-q32.1 region in a patient with normal intelligence.  [electronic resource] 

 -  European journal of medical genetics  Feb 2014 
 - 60-4 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2014.01.006  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple<br/>Adult<br/>Chromosome Banding<br/>Chromosome Deletion<br/>Chromosome Disorders--diagnosis<br/>Chromosomes, Human, Pair 13<br/>Comparative Genomic Hybridization<br/>Facies<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Phenotype<br/>Polymorphism, Single Nucleotide