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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
Methods in Molecular Biology, ISSN 1064-3745, 2017, Volume 1541, pp. 1 - 10
The Philadelphia chromosome was the first chromosomal abnormality discovered in cancer using the cytogenetics technique in 1960, and was consistently... 
FISH | Cancer cytogenetics | Molecular cytogenetics | Review | Karyotyping | Computational Biology - methods | Animals | Comparative Genomic Hybridization | Neoplasms - genetics | Humans | Chromosome Aberrations | Cytogenetics - methods | Databases, Genetic | In Situ Hybridization, Fluorescence | Neoplasms - diagnosis | Genomics - methods
Journal Article
Journal Article