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1. Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.

Authors: A J Mears; T Jordan; F Mirzayans; S Dubois; T Kume; M Parlee; R Ritch; B Koop; W L Kuo; C Collins; J Marshall; D B Gould; W Pearce; P Carlsson; S Enerbäck; J Morissette; S Bhattacharya; B Hogan; V Raymond; M A Walter
Journal: Am J Hum Genet Date: 1998-11 Impact factor: 11.025

2. Familial glaucoma iridogoniodysplasia maps to a 6p25 region implicated in primary congenital glaucoma and iridogoniodysgenesis anomaly.

Authors: T Jordan; N Ebenezer; R Manners; J McGill; S Bhattacharya
Journal: Am J Hum Genet Date: 1997-10 Impact factor: 11.025

3. Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25.

Authors: A J Mears; F Mirzayans; D B Gould; W G Pearce; M A Walter
Journal: Am J Hum Genet Date: 1996-12 Impact factor: 11.025

4. Congenital rubella syndrome.

Authors: A M Brooks; W E Gillies
Journal: Br J Ophthalmol Date: 1994-01 Impact factor: 4.638

5. Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanning.

Authors: F Mirzayans; A J Mears; S W Guo; W G Pearce; M A Walter
Journal: Am J Hum Genet Date: 1997-07 Impact factor: 11.025

5 in total