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Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
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Bilateral Hearing Loss and Constricted Visual Fields
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Muscular Dystrophies
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A Neonate with Micrognathia and Hypotonia
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Hydrocephalus in Children
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Molybdenum Cofactor Deficiency
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Somatic Mutations in Cerebral Cortical Malformations
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Sturge-Weber Syndrome
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The Floppy Infant: Evaluation of Hypotonia
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Developmental Dyslexia
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Multiminicore Disease in a Family Susceptible to Malignant Hyperthermia: Histology, In Vitro Contracture Tests, and Genetic Characterization
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Recessive Ataxia With Ocular Apraxia
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Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
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Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
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Inherited Prothrombotic States and Ischaemic Stroke in Childhood
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Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
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Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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Stroke in Williams Syndrome
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X-Linked Malformation of Neuronal Migration
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Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
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Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
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Familial Autoimmune Myasthenia Gravis
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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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On the Inheritance of Intracranial Aneurysms
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