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J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996
Retinitis Pigmentosa
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Unusual Variants of Alexander's Disease
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
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Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
NEJM 325:1673-1681, Rousseau,F.,et al, 1991
Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence
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Cytomegalovirus and Rasmussen's Encephalitis
Lancet 336:1282-1284, Power,C.,et al, 1990
Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
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