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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (8)
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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, aniridia48040 Foxf2: A novel locus for anterior segment dysgenesis adjacent to the FOXC1 gene
McKeone R; Vieira H; Gregory-Evans K; Gregory-Evans CY; Denny P
PLoS ONE 2011; 6:10 Article Number: e25489
47627 CYP1B1-related anterior segment developmental anomalies: Novel mutations for infantile glaucoma and von Hippel's ulcer revisited
Kelberman D; Islam L; Jacques TS; Russell-Eggitt I; Bitner-Glindzicz M; Khaw PT; Nischal KK; Sowden JC
Ophthalmology 2011; 118: 1865-1873
47656 Unusual presentation in Axenfeld-Rieger syndrome
Parikh RS; Parikh SR; Debashish B; Harsha BL; Thomas R
Indian Journal of Ophthalmology 2011; 59: 312-314
47503 Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma
Khan K; Rudkin A; Parry DA; Burdon KP; McKibbin M; Logan CV; Abdelhamed ZIA; Muecke JS; Fernandez-Fuentes N; Laurie KJ
American Journal of Human Genetics 2011; 89: 464-473
47757 Congenital aniridia
Angmo D; Jha B; Panda A
Journal of Current Glaucoma Practice 2011; 5: 1-13
47844 Glaucoma and frequency of ocular and general diseases in 30 patients with Aniridia: A clinical study
Gramer E; Reiter C; Gramer G
European Journal of Ophthalmology 2011; 22: 104-110
48277 Axenfeld-rieger syndrome in monozygotic twins
Ma J; Zhong Y; Zhao C; Zhang X; Sui R; Chu P; Zhao J
Journal of Glaucoma 2011; 20: 584-586
48397 Should unilateral congenital corneal opacities in Peters' anomaly be grafted?
Basdekidou C; Dureau P; Edelson C; De Laage De Meux P; Caputo G
European Journal of Ophthalmology 2011; 21: 695-699
