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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (5)
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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, aniridia14285 Primary congenital glaucoma and Rieger's anomaly: Extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations
Chavarria Soley G; Michels Rautenstrauss K; Pasutto F; Flikier D; Flikier P; Cirak S; Bejjani B; Winters DL; Lewis RA; Mardin C
Molecular Vision 2006; 12: 523-531
14286 Further support of the role of CYP1B1 in patients with Peters anomaly
Vincent A; Billingsley G; Priston M; Glaser T; Oliver E; Walter M; Ritch R; Levin A; Heon E
Molecular Vision 2006; 12: 506-510
14283 Novel mutations of the PAX6 gene identified in Chinese patients with aniridia
Wang P; Guo X; Jia X; Li S; Xiao X; Zhang Q
Molecular Vision 2006; 12: 644-648
14299 Morphology, family history, and age at diagnosis of 26 patients with Axenfeld-Rieger syndrome and glaucoma or ocular hypertension
Dressler P; Gramer E
Ophthalmologe 2006; 103: 393-400
14178 Strabismus and amblyopia in bilateral Peters anomaly
Najjar DM; Christiansen SP; Bothun ED; Summers CG
Journal of AAPOS 2006; 10: 193-197
