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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (7)
Showing records 1 to 7
Display all abstracts in classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia
Search within classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia16986 Long-term results of surgery in childhood glaucoma
Alsheikheh A; Klink J; Klink T; Steffen H; Grehn F
Graefe's Archive for Clinical and Experimental Ophthalmology 2007; 45: 195-203
16993 Glaucoma in aniridia
Bremond-Gignac D
Journal Français d'Ophtalmologie 2007; 30: 196-199
17117 Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report
de la Houssaye G; Bieche I; Roche O; Vieira V; Laurendeau I; Arbogast L; Zeghidi H; Rapp P; Halimi P; Vidaud M
BMC Medical Genetics 2006; 7: 82
16990 Gillespie syndrome: an uncommon presentation of congenital aniridia
Defreyn A; Maugery J; Chabrier S; Coullet J
Journal Français d'Ophtalmologie 2007; 30: e1
17006 Glaucoma with aniridia and isolated congenital glaucoma in siblings: contribution and limits of genetics
Lise-Schneider B; Calvas P; Roche O; Lambert JC; Dufier JL; Costet-Fighiera C
Journal Français d'Ophtalmologie 2007; 30: 44-48
17015 Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations
Strungaru MH; Dinu I; Walter MA
Investigative Ophthalmology and Visual Science 2007; 48: 228-237
17189 Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome
Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF
Molecular Vision 2006; 12: 1448-1460
