Chromosomal Duplication Involving the Forkhead Transcription Factor GeneFOXC1Causes Iris Hypoplasia and Glaucoma
- 1 November 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 67 (5) , 1129-1135
- https://doi.org/10.1086/321194
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakageHuman Molecular Genetics, 2000
- Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25European Journal of Human Genetics, 2000
- Glaucoma genetics: where are we? where will we go?Current Opinion in Opthalmology, 1999
- Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger AnomalyAmerican Journal of Human Genetics, 1998
- The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25Nature Genetics, 1998
- Familial Glaucoma Iridogoniodysplasia Maps to a 6p25 Region Implicated in Primary Congenital Glaucoma and Iridogoniodysgenesis AnomalyAmerican Journal of Human Genetics, 1997
- Influence of PAX6 Gene Dosage on Development: Overexpression Causes Severe Eye AbnormalitiesCell, 1996
- Number of people with glaucoma worldwide.British Journal of Ophthalmology, 1996
- DNA duplication associated with Charcot-Marie-Tooth disease type 1ACell, 1991
- Differential DNA sequence deletions from chromosomes 3, 11, 13, and 17 in squamous-cell carcinoma, large-cell carcinoma, and adenocarcinoma of the human lung.Proceedings of the National Academy of Sciences, 1989