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Mutations in ASCC3L1 on chromosome 2q11.2 are associated with autosomal dominant retinitis pigmentosa in a Chinese Family
Investigative Ophthalmology and Visual Science, 09/04/09
Li N et al. – These results provide strong evidence that mutations in ASCC3L1 result in autosomal dominant retinitis pigmentosa in this Chinese family.
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MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma
Molecular Vision, 11/09/09
IL-33 shifts macrophage polarization, promoting resistance against Pseudomonas aeruginosa keratitis
Investigative Ophthalmology and Visual Science, 11/23/09
Understanding ischemic retinopathies: emerging concepts from oxygen-induced retinopathy
Documenta Ophthalmologica, 11/03/09
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Value of retinal examination in hypertensive encephalopathy
Journal of Human Hypertension, 11/03/09
Retinopathy of Prematurity
NeoReviews, 11/04/09
Late Increased Risk of Retinal Detachment after Cataract Extraction
American Journal of Ophthalmology, 10/30/09
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