MeSH term
Frequency | Condition_Probility | Adolescent | 7 | 0.0 |
Alleles | 4 | 0.0 |
Exons | 3 | 0.0 |
Female | 18 | 0.0 |
Genotype | 6 | 0.0 |
Humans | 25 | 0.0 |
Male | 18 | 0.0 |
Polymorphism, Genetic | 2 | 0.0 |
Receptors, GABA-A/*genetics | 14 | 18.0 |
Research Support, Non-U.S. Gov't | 19 | 0.0 |
Reverse Transcriptase Polymerase Chain Reaction | 2 | 0.0 |
Epilepsy, Generalized/*genetics | 4 | 14.0 |
Mutation/genetics | 2 | 0.0 |
Nerve Tissue Proteins/*genetics | 3 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 6 | 0.0 |
Sodium Channels/*genetics | 3 | 3.0 |
Amino Acid Sequence | 3 | 0.0 |
Child, Preschool | 5 | 0.0 |
DNA Mutational Analysis | 5 | 0.0 |
Genetic Predisposition to Disease | 3 | 0.0 |
Infant | 3 | 0.0 |
Molecular Sequence Data | 8 | 0.0 |
*Mutation | 4 | 0.0 |
Phenotype | 6 | 0.0 |
Adult | 7 | 0.0 |
Child | 7 | 0.0 |
Comparative Study | 3 | 0.0 |
Electroencephalography | 4 | 1.0 |
Family | 2 | 0.0 |
Linkage (Genetics) | 5 | 0.0 |
Lod Score | 2 | 0.0 |
Pedigree | 8 | 0.0 |
Base Sequence | 6 | 0.0 |
DNA | 2 | 0.0 |
Introns | 2 | 0.0 |
Age of Onset | 2 | 0.0 |
Chromosome Segregation | 2 | 5.0 |
Epilepsy, Absence/*genetics | 2 | 11.0 |
Protein Subunits | 3 | 0.0 |
Seizures, Febrile/*genetics | 5 | 27.0 |
Epilepsy/*genetics | 2 | 6.0 |
Chromosome Mapping | 4 | 0.0 |
*Chromosomes, Human, Pair 5 | 4 | 1.0 |
*Polymorphism, Genetic | 3 | 0.0 |
Polymorphism, Restriction Fragment Length | 2 | 0.0 |
Animals | 2 | 0.0 |
Chromosomes, Human, Pair 5/*genetics | 3 | 3.0 |
Polymerase Chain Reaction | 3 | 0.0 |
Polymorphism, Single Nucleotide/genetics | 2 | 0.0 |
Variation (Genetics) | 2 | 0.0 |
Middle Aged | 4 | 0.0 |
Mutation | 2 | 0.0 |
Epilepsy, Absence/genetics | 2 | 66.0 |
Linkage (Genetics)/*genetics | 2 | 0.0 |
Multigene Family | 2 | 0.0 |
*Multigene Family | 2 | 0.0 |
Haplotypes | 2 | 0.0 |
DNA/genetics | 3 | 0.0 |
Gene Frequency/genetics | 2 | 0.0 |
Genetic Screening | 2 | 0.0 |
Linkage Disequilibrium | 2 | 0.0 |
Polymorphism, Genetic/genetics | 5 | 0.0 |
