Córdova-Fletes, Carlos <br/><br/>
A del(13)(q21.32q31.2)dn refined to 21.9 Mb in a female toddler with irides heterochromia and hypopigmentation: appraisal of interstitial mid-13q deletions.  [electronic resource] 

 -  Clinical dysmorphology  Jan 2017 
 - 33-37 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1473-5717 
<br/><br/><label>Standard No.: </label>10.1097/MCD.0000000000000159  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Brain--pathology<br/>Child<br/>Child, Preschool<br/>Chromosome Banding<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 13<br/>Comparative Genomic Hybridization<br/>Female<br/>Genetic Association Studies<br/>Humans<br/>Hypopigmentation--diagnosis<br/>Iris Diseases--diagnosis<br/>Magnetic Resonance Imaging<br/>Phenotype<br/>Pigmentation Disorders--diagnosis