Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022
A Neonate with Micrognathia and Hypotonia
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Prader-Willi and Angelman Syndromes
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Fucosidosis Revisited:A Review of 77 Patients
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Physical Features of Prader-Willi Syndrome in Neonates
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Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
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