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Neurological Involvement in the Epidermal Naevus Syndrome
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Rubella, Clinical Manifestations & Management
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An 11-year-old Boy with Language Disorder and Epilepsy
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Newborn Screening for Fragile X Syndrome
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Febrile Infection-Related Epilepsy Syndrome: A Study of 12 Patients
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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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Overview of Phenylketonuria
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Angelman Syndrome Revisited
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Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
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Developmental Neurotoxivity of Industrial Chemicals
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Mental Retardation
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Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
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Prader-Willi and Angelman Syndromes
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The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
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Startle Provoked Epileptic Seizures:Features in 19 Patients
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Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
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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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Neurodevelopmental Outcome of Infants with Hypoplastic Left Heart Syndrome
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Rapid Antibody Test for Fragile X Syndrome
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Neurologic Abnormalities in Murderers
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Advances in Molecular Analysis of Fragile X Syndrome
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Do Young Boys with Fragile X Syndrome have Macroorchidism
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Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
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Molecular Genetic Advances in Fragile X Syndrome
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Fetal Alcohol Syndrome and Fetal Alcohol Effects
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Prenatal Alcohol Exposure and Long-Term Developmental Consequences
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Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
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Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
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Choroido-Cerebral Calcification Syndrome with Retardation
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Mental Development of 2-Year-Old Children Exposed to Alcohol in Utero
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Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
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Detection of Full Fragile X Mutation
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New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Population Screening for Fragile X
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Twinning and Neurologic Morbisity
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Cognitive Assessment of Human Immunodeficiency Virus-Exposed Children
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