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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (4)
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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, aniridia28123 Large novel deletions detected in Chinese families with aniridia: Correlation between genotype and phenotype
Zhang X; Zhang Q; Tong Y; Dai H; Zhao X; Bai F; Xu L; Li Y
Molecular Vision 2011; 17: 548-557
28236 Reiger anomaly due to a FOXC1 gene deletion: Look beyond the eyes
Hanna B; Rajagopalan S
Twin Research and Human Genetics: the Official Journal of the International Society for Twin Studies 2010; 13: 642
28179 Posterior migration of Ahmed glaucoma valve tube in a patient with Reiger anomaly: a case report
Gupta VS; Sethi HS; Gupta M; Mehta A; Singh S; Yadav P; Malik KP
BMC Ophthalmology 2010; 10: 23
28164 Clinical spectrum of type IV collagen (COL4A1) mutations: A novel genetic multisystem disease
Vahedi K; Alamowitch S
Current Opinion in Neurology 2011; 24: 63-68
