Şimşek-Kiper, Pelin Özlem <br/><br/>
A de novo 11q23 deletion in a patient presenting with severe ophthalmologic findings, psychomotor retardation and facial dysmorphism.  [electronic resource] 

 -  The Turkish journal of pediatrics   
 - 80-4 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>2791-6421 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Child, Preschool<br/>Craniofacial Abnormalities<br/>Face--abnormalities<br/>Facies<br/>Female<br/>Humans<br/>Jacobsen Distal 11q Deletion Syndrome<br/>Muscular Atrophy--genetics<br/>Ophthalmoplegia--genetics<br/>Psychomotor Disorders--genetics