Links
[1] https://disorders.eyes.arizona.edu/disorders/aniridia
[2] http://omim.org/entry/106210
[3] https://disorders.eyes.arizona.edu/disorders/peters-anomaly
[4] http://omim.org/entry/604229
[5] https://disorders.eyes.arizona.edu/disorders/iridogoniodysgenesis-type-1
[6] http://omim.org/entry/601631
[7] https://disorders.eyes.arizona.edu/disorders/iridogoniodysgenesis-type-2
[8] http://omim.org/entry/137600
[9] http://ghr.nlm.nih.gov/gene/PITX3
[10] http://ghr.nlm.nih.gov/gene/FOXE3
[11] https://disorders.eyes.arizona.edu/disorders/aphakia-congenital-primary
[12] http://omim.org/entry/610256
[13] https://disorders.eyes.arizona.edu/disorders/anterior-segment-dysgenesis-6
[14] http://omim.org/entry/617315
[15] https://disorders.eyes.arizona.edu/disorders/anterior-segment-dysgenesis-8
[16] http://omim.org/entry/617319
[17] https://disorders.eyes.arizona.edu/references/novel-non-stop-mutation-foxe3-causes-autosomal-dominant-form-variable-anterior-segment
[18] https://disorders.eyes.arizona.edu/references/anterior-segment-mesenchymal-dysgenesis-large-australian-family-associated-recurrent-17