| 1 | IHG2, PITX2 |
| Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene. | |
| Alward WL, Semina EV, Kalenak JW, Heon E, Sheth BP, Stone EM, Murray JC. | |
| Am J Ophthalmol 125(1):98-100. 1998 | |
| 2 | IHG2, PITX2 |
| Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome. | |
| Kulak SC, Kozlowski K, Semina EV, Pearce WG, Walter MA. | |
| Hum Mol Genet 7(7):1113-7. 1998 | |
| 3 | IHG2, RIEG1 |
| Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25). | |
| HŽon E, et al. | |
| Hum Mol Genet 4 : 1435-1439. 1995 | |