No abstract available
MeSH terms
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Abnormalities, Multiple / genetics*
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Child
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Chromosomes, Human, Pair 4*
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Chromosomes, Human, Pair 9*
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Epilepsies, Partial / diagnosis
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Epilepsies, Partial / genetics*
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Female
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Humans
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In Situ Hybridization, Fluorescence
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Intellectual Disability / diagnosis
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Intellectual Disability / genetics*
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Neurologic Examination
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Nuclear Proteins / genetics
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Phenotype
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Translocation, Genetic*
Substances
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MLLT3 protein, human
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Nuclear Proteins