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Recurrent Cerebral Ischemia During Pregnancies
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Ehlers-Danlos Syndromes
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Genetic Aspects of Alzheimer Disease
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The Tuberous Sclerosis Complex
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Sensorineural Hearing Loss in Children
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Prader-Willi and Angelman Syndromes
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Clinical Genetics in Neurological Disease
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
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Unstable DNA Sequence in Myotonic Dystrophy
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De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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Molecular Genetics of Duchenne and Becker Muscular Dystrophy
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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Predictive Testing for Huntington's Disease, Progress and Problems
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Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
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Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
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Anderson-Fabray Disease, A Commonly Missed Diagnosis
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Fibromuscular Dysplasia and Its Neurologic Manifestations
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Degenerative Diseases of the Nervous System, Parkinson Disease
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Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
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Dopa-Responsive Dystonia Revisited
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