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Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study
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Transition to Adult Care for Children with Chronic Neurological Disorders
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Extension of the Clinical Spectrum of Danon Disease
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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The Relation of Transient Hypothyroxinemia in Preterm Infants to Neurologic Development at Two Years of Age
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Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
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Prenatal Magnesium Sulfate Expos/Risk for CP or MR Among Very Low-Birth-Weight Child Aged 3-5 Yrs
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A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
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Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
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Rapid Antibody Test for Fragile X Syndrome
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Alternating Hemiplegia in Infants:Report of Five Cases
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