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Publications by G. C. M. Black
The Phenotypic Variability of Retinal Dystrophies Associated With Mutations in CRX, With Report of a Novel Macular Dystrophy Phenotype
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
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Phenotypic Variability Due to a Novel Glu292Lys Variation in Exon 8 of the BEST1 Gene Causing Best Macular Dystrophy
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Identifying Mutations in Tunisian Families With Retinal Dystrophy
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Detailed Functional and Structural Phenotype of Bietti Crystalline Dystrophy Associated With Mutations in CYP4V2 Complicated by Choroidal Neovascularization
Ophthalmic Genetics
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Hypotrichosis With Juvenile Macular Dystrophy
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Features Associated With Foveal Retinal Detachment in Myopic Macular Retinoschisis
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Identification of Two Novel LAMA2 Mutations in a Chinese Patient With Congenital Muscular Dystrophy
Frontiers in Genetics
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Macular Dystrophy in Kjellin’s Syndrome: A Case Report
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Unusual Macular Retinal Detachment Associated With Vitreomacular Traction Syndrome
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Molecular Neuroscience
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Macular Buckling Surgery for Retinal Detachment Associated With Macular Hole in High Myopia Eye
Turk Oftalmoloiji Dergisi
Ophthalmology
