No abstract available
MeSH terms
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Abnormalities, Multiple*
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Auditory Perceptual Disorders / diagnosis
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Auditory Perceptual Disorders / genetics
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Corneal Dystrophies, Hereditary / diagnosis
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Corneal Dystrophies, Hereditary / genetics*
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Craniofacial Abnormalities / genetics
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Empty Sella Syndrome / genetics
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Endothelium, Corneal / abnormalities*
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Eye Abnormalities / diagnosis
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Eye Abnormalities / genetics*
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Eye Proteins / genetics*
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Homeodomain Proteins / genetics*
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Humans
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Keratoconus / diagnosis
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Keratoconus / genetics*
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Mutation*
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Retinal Diseases / diagnosis
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Retinal Diseases / genetics
Substances
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Eye Proteins
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Homeodomain Proteins
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VSX1 protein, human