Kraoua, Lilia <br/><br/>
Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case report.  [electronic resource] 

 -  European journal of medical genetics   
 - e446-50 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.2011.04.007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Angelman Syndrome--genetics<br/>Chromosome Banding<br/>Chromosome Disorders--genetics<br/>Chromosomes, Human, Pair 15--genetics<br/>Humans<br/>Male<br/>Membrane Transport Proteins--genetics<br/>Phenotype<br/>Pigmentation Disorders--genetics<br/>Prader-Willi Syndrome--genetics