Tarlan, Berçin <br/><br/>
A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.  [electronic resource] 

 -  Ophthalmic genetics  Dec 2014 
 - 248-51 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1744-5094 
<br/><br/><label>Standard No.: </label>10.3109/13816810.2013.811269  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple<br/>Aphakia--congenital<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22--genetics<br/>Consanguinity<br/>Corneal Diseases--diagnosis<br/>Developmental Disabilities--diagnosis<br/>DiGeorge Syndrome--diagnosis<br/>Growth Disorders--diagnosis<br/>Heart Septal Defects, Ventricular--diagnosis<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Kidney--abnormalities<br/>Magnetic Resonance Imaging<br/>Male<br/>Microphthalmos--diagnosis