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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Molybdenum Cofactor Deficiency
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
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A Clinical Study of Noonan Syndrome
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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Anderson-Fabray Disease, A Commonly Missed Diagnosis
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Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
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