大家都搜:
[眼科]睑裂狭小
1、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。
2、Clinical characteristics and surgical treatment of congenital blepharophimosis syndrome───先天性小睑裂综合症的临床特征与手术治疗
3、Triple plasitc surgery for congenital blepharophimosis───三联术治疗先天性睑裂狭小综合征
4、Objective to evaluate the surgical results of blepharophimosis-ptosis-epicanthus inversus syndrome (BPES).───目的探讨小睑裂综合征的联合手术方法。
1、Objective To screen mutations in the forkhead transcriptional factor 2 gene (FOXL2) in six Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome(BPES).