Links
[1] http://ghr.nlm.nih.gov/gene/PRDM5
[2] https://ghr.nlm.nih.gov/gene/CYP1B1
[3] http://ghr.nlm.nih.gov/gene/PITX2
[4] http://ghr.nlm.nih.gov/gene/FOXC1
[5] https://disorders.eyes.arizona.edu/disorders/axenfeld-rieger-syndrome-type-1
[6] http://omim.org/entry/180500
[7] https://disorders.eyes.arizona.edu/disorders/axenfeld-rieger-syndrome-type-2
[8] http://www.ncbi.nlm.nih.gov/omim/601499
[9] https://disorders.eyes.arizona.edu/disorders/axenfeld-rieger-syndrome-type-3
[10] http://www.ncbi.nlm.nih.gov/omim/602482
[11] https://disorders.eyes.arizona.edu/disorders/brittle-cornea-syndrome-2
[12] http://omim.org/entry/614170
[13] https://disorders.eyes.arizona.edu/references/whole-exome-sequencing-identifies-heterozygous-missense-variant-prdm5-gene-family-axenfel