Late-onset Lennox-Gastaut syndrome in a patient with 15q11.2-q13.1 duplication
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference9 articles.
1. The inv dup(15) or idic(15) syndrome: A clinically recognizable neurogenetic disorder;Battaglia;Neurology,1997
2. 15q 11-13 GABA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders;Hogart;Hum Mol Genet,2007
3. The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13;Hogart;Neurobiol Dis
4. Autism spectrum disorders;Lord;Neuron,2000
5. Supernumerary tricentric derivative chromosome 15 in two boys with intractable epilepsy: another mechanism for partial hexasomy;Mann;Hum Genet,2004
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3. Electro-clinical features in epileptic children with chromosome 15q duplication syndrome;Clinical Neurophysiology;2021-05
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