Lennon, P A <br/><br/>
WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jun 2006 
 - 1214-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.31229  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Blepharoptosis--pathology<br/>Chromosome Banding<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 11--genetics<br/>Chromosomes, Human, Pair 15--genetics<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Karyotyping<br/>Obesity--pathology<br/>Translocation, Genetic<br/>WAGR Syndrome--pathology