Kraoua, L <br/><br/>
FOXL2 mutations in Tunisian patients with blepharophimosis-ptosis-epicanthus inversus syndrome.  [electronic resource] 

 -  Clinical genetics  Jun 2010 
 - 601-3 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2010.01389.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Blepharophimosis--genetics<br/>Blepharoptosis--genetics<br/>Child<br/>Eyelid Diseases--genetics<br/>Female<br/>Forkhead Box Protein L2<br/>Forkhead Transcription Factors--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Syndrome<br/>Tunisia