Fig. 4From: Novel FOXL2 mutations in two Chinese families with blepharophimosis-ptosis-epicanthus inversus syndromeSequencing results of the two novel mutations in FOXL2 (the heterozygous mutation c.675_690delinsT in family a and the missense mutation (c.223C > T) in family b). The mutant alleles identified in the present study are compared with the normal alleles. The red marks indicate the position of mutationsBack to article page