目的对小睑裂综合征家系患者的FOXL2基因突变进行研究，寻找突变位点。
Objective To screen mutations in the forkhead transcriptional factor 2 gene (FOXL2) in six Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome(BPES).
目的对小睑裂综合征家系患者的FOXL2基因突变进行研究，寻找突变位点。
Objective To screen mutations in the forkhead transcriptional factor 2 gene (FOXL2) in six Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome(BPES).
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