A Child with Arthrogryposis
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A Neonate with Micrognathia and Hypotonia
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
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Juvenile Diabetes Mellitus & Optic Atrophy
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