Chromosomal Duplication Involving the Forkhead Transcription Factor Gene FOXC1 Causes Iris Hypoplasia and Glaucoma

This publication has 13 references indexed in Scilit:

• Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakage
  Human Molecular Genetics, 2000
• Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25
  European Journal of Human Genetics, 2000
• An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2alpha that affects anterior eye chamber development.
  1999
• Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly
  American Journal of Human Genetics, 1998
• The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
  Nature Genetics, 1998
• Familial Glaucoma Iridogoniodysplasia Maps to a 6p25 Region Implicated in Primary Congenital Glaucoma and Iridogoniodysgenesis Anomaly
  American Journal of Human Genetics, 1997
• Number of people with glaucoma worldwide.
  British Journal of Ophthalmology, 1996
• DNA duplication associated with Charcot-Marie-Tooth disease type 1A
  Cell, 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
• Easy calculations of lod scores and genetic risks on small computers.
  1984