Laimutis, Kucinskas <br/><br/>
Typical renal-coloboma syndrome phenotype in a patient with a submicroscopic deletion of the PAX2 gene.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jun 2012 
 - 1437-41 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.35342  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Biopsy<br/>Child<br/>Child, Preschool<br/>Coloboma--diagnosis<br/>Glomerulosclerosis, Focal Segmental--pathology<br/>Humans<br/>Infant<br/>Kidney--diagnostic imaging<br/>PAX2 Transcription Factor--genetics<br/>Phenotype<br/>Renal Insufficiency--diagnosis<br/>Sequence Deletion<br/>Ultrasonography<br/>Vesico-Ureteral Reflux--diagnosis