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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Molybdenum Cofactor Deficiency
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Sturge-Weber Syndrome
UptoDate , Nov, Bodensteiner, J.B., 2014
Sturge-Weber Syndrome
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Gray Matter Heterotopias:MR Characteristics & Correlation with Develop & Neurologic Manifest
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A Clinical Study of Noonan Syndrome
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Prospective Observations of 100 High-Risk Neonates by High-Field MRI of CNS:I. Intraventricular & Extracerebral Lesions
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Fucosidosis Revisited:A Review of 77 Patients
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Thalamic Hemorrhage with Intraventricular Hemorrhage in the Full-Term Newborn
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