Nallathambi, Jeyabalan <br/><br/>
FOXL2 mutations in Indian families with blepharophimosis-ptosis-epicanthus inversus syndrome.  [electronic resource] 

 -  Journal of genetics  Aug 2007 
 - 165-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0022-1333 
<br/><br/><label>Standard No.: </label>10.1007/s12041-007-0021-z  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blepharophimosis--complications<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Eye Diseases--congenital<br/>Family<br/>Female<br/>Forkhead Box Protein L2<br/>Forkhead Transcription Factors--genetics<br/>Humans<br/>India<br/>Infant<br/>Male<br/>Mutation<br/>Pedigree<br/>Syndrome