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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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Somatic Mutations in Cerebral Cortical Malformations
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Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
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Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
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Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
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Genomewide Association Studies of Stroke
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
Eur J Neurol 16:513-516, Lee, Y.-C.,et al, 2009
Impact of the Human Genome Projects and Identification of a Stroke Gene
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Complete Genomic Screen in Parkinson Disease
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The Brain Code in Health and Disease
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Multiple Sclerosis
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The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
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Conjugal Multiple Sclerosis:A Clinical and Laboratory Study
Neurol 41:1320-1321, Finelli,P.F., 1991
Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients
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Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990
Risk Factors for Multiple Sclerosis:Race or Place? Editorial
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Familial Patterns of Narcolepsy
lancet 2:1376-1379, Guilleminault,C.,et al, 1989
Genetic Factors in Myasthenia Gravis:A Family Study
Neurol 38:38-42, Kerzin-Storrar,L.,et al, 1988
Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
NEJM 318:684-688, Martuza,R.L.&Eldridge,R., 1988
Narcolepsy & Immunity
BMJ 292:359-360, Parkes,J.D.,et al, 1986
The Genetics of Susceptibility to Multiple Sclerosis
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A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980
Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977
Cause of Weakness in Myasthenia Gravis
NEJM 294:722, Grob,D., 1976
Nerve-Growth Factor in Familial Dysautonomia
NEJM 295:671, Montalcini,R.L., 1976