Links
[1] http://ghr.nlm.nih.gov/gene/CHRDL1
[2] http://disorders.eyes.arizona.edu/disorders/marfan-syndrome
[3] http://www.ncbi.nlm.nih.gov/omim/154700
[4] http://disorders.eyes.arizona.edu/disorders/axenfeld-rieger-syndrome-type-1
[5] http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180500
[6] http://disorders.eyes.arizona.edu/disorders/neuhauser-syndrome
[7] http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=249310
[8] http://ghr.nlm.nih.gov/gene/LTBP2
[9] https://disorders.eyes.arizona.edu/disorders/megalocornea-ectopia-lentis-and-spherophakia
[10] https://disorders.eyes.arizona.edu/references/association-chrdl1-mutations-and-variants-x-linked-megalocornea-neuh%C3%A4user-syndrome-and-ce
[11] https://disorders.eyes.arizona.edu/references/x-linked-megalocornea-caused-mutations-chrdl1-identifies-essential-role-ventroptin
[12] https://disorders.eyes.arizona.edu/references/congenital-megalocornea-zonular-weakness-and-childhood-lens-related-secondary-glaucoma
[13] https://disorders.eyes.arizona.edu/references/description-x-linked-megalocornea-identification-gene-locus
[14] https://disorders.eyes.arizona.edu/references/x-linked-megalocornea-close-linkage-dxs87-and-dxs94
[15] https://disorders.eyes.arizona.edu/references/syndrome-mental-retardation-seizures-hypotonic-cerebral-palsy-and-megalocorneae