MeSH term
Frequency | Condition_Probility | Adolescent | 2 | 0.0 |
Adult | 5 | 0.0 |
Epilepsy, Generalized/etiology/genetics | 2 | 100.0 |
Genetic Predisposition to Disease | 3 | 0.0 |
Humans | 14 | 0.0 |
Molecular Sequence Data | 5 | 0.0 |
Myoclonic Epilepsy, Juvenile/etiology/*genetics | 2 | 100.0 |
Pedigree | 5 | 0.0 |
Receptors, GABA-A/*genetics | 8 | 10.0 |
Research Support, Non-U.S. Gov't | 9 | 0.0 |
Analysis of Variance | 2 | 0.0 |
Female | 10 | 0.0 |
Genotype | 5 | 0.0 |
Haplotypes | 2 | 0.0 |
Male | 10 | 0.0 |
Polymorphism, Genetic/genetics | 3 | 0.0 |
Middle Aged | 4 | 0.0 |
Polymorphism, Genetic | 3 | 0.0 |
Base Sequence | 4 | 0.0 |
*Chromosomes, Human, Pair 5 | 4 | 1.0 |
Family | 2 | 0.0 |
Linkage (Genetics)/*genetics | 2 | 0.0 |
Animals | 3 | 0.0 |
Chromosome Mapping | 2 | 0.0 |
Hamsters | 2 | 0.0 |
Hybrid Cells | 2 | 0.0 |
Alleles | 2 | 0.0 |
DNA Mutational Analysis | 2 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 3 | 0.0 |
*Linkage (Genetics) | 2 | 0.0 |
Linkage Disequilibrium | 2 | 0.0 |