Prenatal diagnosis of aniridia
- 30 June 2000
- journal article
- Published by Elsevier in Ophthalmology
- Vol. 107 (6) , 1153-1156
- https://doi.org/10.1016/s0161-6420(00)00093-2
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Polymerase Chain Reaction–Based Risk Assessment for Wilms Tumor in Sporadic AniridiaAmerican Journal of Ophthalmology, 1998
- PAX6 mutations reviewedHuman Mutation, 1998
- The incidence of PAX6 mutation in patients with simple aniridia: an evaluation of mutation detection in 12 cases.Journal of Medical Genetics, 1997
- PAX6 missense mutation in isolated foveal hypoplasiaNature Genetics, 1996
- Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomalyNature Genetics, 1994
- Attitudes towards prenatal diagnosis and selective abortion among patients with retinitis pigmentosa or choroideremia as well as among their relativesClinical Genetics, 1993
- Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 geneNature Genetics, 1992
- Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia regionCell, 1991