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Hyperostosis Cranialis Interna
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Refsum Disease
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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Hereditary Neuropathy with Liability to Pressure Palsies
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Famillial Carpal Tunnel Syndrome
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Gyrate Atrophy of the Choroid & Retina with Hyperornithinemia:Tubular Aggreg. & Type 2 Fiber Atrophy
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Genetic Counseling in Retinitis Pigmentosa
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