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LANCET NEUROLOGY, ISSN 1474-4422, 08/2018, Volume 17, Issue 8, pp. 657 - U3
William Lennox studied twins with epilepsy as early as the 1930s and found a high concordance rate between monozygotic twins; later twin studies confirmed his... 
CLINICAL NEUROLOGY | TWINS | MUTATION | Studies | γ-Aminobutyric acid | Genomes | Epilepsy | Genes
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2014, Volume 23, Issue 12, pp. 3200 - 3211
Journal Article
Genome Medicine, ISSN 1756-994X, 08/2015, Volume 7, Issue 1, p. 91
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 11/2012, Volume 367, Issue 20, pp. 1951 - 1953
Journal Article
Epilepsy and Behavior, ISSN 1525-5050, 2014, Volume 41, pp. 276 - 276
Journal Article
Epilepsy Currents, ISSN 1535-7597, 9/2019, Volume 19, Issue 5, pp. 307 - 309
Diagnostic Exome Sequencing in 100 Consecutive Patients With Both Epilepsy and Intellectual Disability Snoeijen-Schouwenaars FM, van Ool JS, Verhoeven JS, et... 
CLINICAL NEUROLOGY
Journal Article
Science, ISSN 0036-8075, 12/2012, Volume 338, Issue 6114, pp. 1619 - 1622
Journal Article
Epilepsia, ISSN 0013-9580, 03/2011, Volume 52, Issue 3, pp. 423 - 432
Summary We set out to review the extent to which molecular karyotyping has overtaken conventional cytogenetics in applications related to epilepsy. Multiplex... 
15q11.2 | Microdeletion | 16p13.11 | Copy number variant (CNV) | 15q13.3 | 15q11 | 16p13 | FAMILIAL NEONATAL SEIZURES | 15q13 | FRONTAL-LOBE EPILEPSY | REFRACTORY EPILEPSY | MENTAL-RETARDATION | POTASSIUM CHANNEL GENE | CLINICAL NEUROLOGY | INTELLECTUAL DISABILITY | IDIOPATHIC GENERALIZED EPILEPSY | EARLY-ONSET | SEVERE MYOCLONIC EPILEPSY | COMPARATIVE GENOMIC HYBRIDIZATION | Gene Frequency - genetics | Chromosome Duplication | Humans | Genetic Counseling | Intellectual Disability - genetics | Karyotyping | Epilepsy - genetics | Cytogenetic Analysis | Chromosomes, Human, Pair 16 - genetics | Chromosome Deletion | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Chromosome Banding | Comorbidity | Exons - genetics | Genotype | DNA Copy Number Variations - genetics | Chromosomes, Human, Pair 15 - genetics | Nerve Tissue Proteins - genetics | Syndrome | NAV1.1 Voltage-Gated Sodium Channel | Phenotype | Comparative Genomic Hybridization | KCNQ2 Potassium Channel - genetics | Sodium Channels - genetics | Receptors, Nicotinic - genetics | Schizophrenia | Cytogenetics | Disease susceptibility | Genomics | Epilepsy | Medical genetics | Genomes | Genetic counseling | DNA probes | Mental disorders | Hot spots | Mental retardation | Pathogenicity | Autism | DNA microarrays | homologous recombination | Sodium channels (voltage-gated) | Potassium channels (voltage-gated) | copy number | KCNQ2 protein
Journal Article
Cell, ISSN 0092-8674, 07/2014, Volume 158, Issue 2, pp. 263 - 276
Journal Article