Autosomal dominant iris hypoplasia is caused by a mutation in the rieger syndrome (rieg/pitx2) gene
- 1 January 1998
- journal article
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 125 (1) , 98-100
- https://doi.org/10.1016/s0002-9394(99)80242-6
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeNature Genetics, 1996
- Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)Human Molecular Genetics, 1995
- Genetic Clues to Glaucoma's SecretsAmerican Journal of Ophthalmology, 1994
- Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4Nature Genetics, 1992
- Familial glaucoma. In nine generations of a South Hampshire family.British Journal of Ophthalmology, 1974