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Expert Review of Ophthalmology, ISSN 1746-9899, 03/2016, Volume 11, Issue 2, pp. 135 - 144
Congenital aniridia manifests as total or partial absence of the iris caused most commonly by mutations in PAX6, FOXC1, PITX2, and CYP1B1. Recently two new... 
congenital | goniotomy | cataract | Aniridia | aniridiaassociated keratopathy
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2016, Volume 98, Issue 5, pp. 971 - 980
Journal Article
Journal of Cataract and Refractive Surgery, ISSN 0886-3350, 2013, Volume 39, Issue 4, pp. 645 - 648
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2016, Volume 98, Issue 5, pp. 981 - 992
Journal Article
Acta Ophthalmologica, ISSN 1755-375X, 2008, Volume 86, Issue 7, pp. 730 - 734
Journal Article
Arquivos Brasileiros de Oftalmologia, ISSN 0004-2749, 2016, Volume 79, Issue 1, pp. 44 - 45
Journal Article