Fig. 4
![Fig. 4](http://media.springernature.com/full/springer-static/image/art%3A10.1186%2Fs12881-015-0217-7/MediaObjects/12881_2015_217_Fig4_HTML.gif)
Sequencing 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 mutations