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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
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De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
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A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24
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The Epilepsy of Trisomy 9p
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New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
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