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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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Sensorineural Hearing Loss in Children
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Prader-Willi and Angelman Syndromes
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The Muscular Dystrophies
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
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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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Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
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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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Genetic Markers for Neurofibromatosis
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Anderson-Fabray Disease, A Commonly Missed Diagnosis
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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Cavernous Maliformations of the Central Nervous System
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Genetics of Cluster Headache Takes a Leap
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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