Links
[1] http://ghr.nlm.nih.gov/gene/KAT6B
[2] http://ghr.nlm.nih.gov/gene/FOXL2
[3] https://disorders.eyes.arizona.edu/references/novel-foxl2-mutations-cause-blepharophimosis-ptosis-epicanthus-inversus-syndrome
[4] https://disorders.eyes.arizona.edu/references/individual-blepharophimosis-ptosis-epicanthus-inversus-syndrome-bpes-and-additional-featu
[5] https://disorders.eyes.arizona.edu/references/notch-foxl2-%C5%93%C2%B1-sma-axis-eyelid-levator-muscle-development-and-congenital-blepharophimosis
[6] https://disorders.eyes.arizona.edu/references/missense-mutation-outside-forkhead-domain-foxl2-causes-severe-form-bpes-type-ii
[7] https://disorders.eyes.arizona.edu/references/difficult-nosology-blepharophimosis%E2%80%9A%C3%A4%C3%ACmental-retardation-syndromes-report-two-siblings
[8] https://disorders.eyes.arizona.edu/references/gene-blepharophimosis-ptosis-epicanthus-inversus-syndrome-maps-chromosome-3q23
[9] https://disorders.eyes.arizona.edu/references/lacrimal-gland-involvement-blepharophimosis-ptosis-epicanthus-inversus-syndrome