Or, Siu-fong June <br/><br/>
Three novel FOXL2 gene mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.  [electronic resource] 

 -  Chinese medical journal  Jan 2006 
 - 49-52 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0366-6999 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Amino Acid Sequence<br/>Blepharophimosis--genetics<br/>Blepharoptosis--genetics<br/>Eyelids--abnormalities<br/>Female<br/>Forkhead Box Protein L2<br/>Forkhead Transcription Factors--genetics<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Syndrome