MeSH term
Frequency | Condition_Probility | Amino Acid Sequence | 2 | 0.0 |
Animals | 4 | 0.0 |
Base Sequence | 3 | 0.0 |
Chromosome Mapping | 8 | 0.0 |
*Chromosomes, Human, Pair 6 | 5 | 1.0 |
Cloning, Molecular | 2 | 0.0 |
Humans | 18 | 0.0 |
Mice | 3 | 0.0 |
Molecular Sequence Data | 5 | 0.0 |
Myoclonic Epilepsy, Juvenile/*genetics | 6 | 54.0 |
Pedigree | 7 | 0.0 |
Research Support, Non-U.S. Gov't | 14 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 3 | 0.0 |
Child | 5 | 0.0 |
Child, Preschool | 3 | 0.0 |
Family | 2 | 0.0 |
Genotype | 5 | 0.0 |
Infant | 2 | 0.0 |
Linkage (Genetics) | 7 | 0.0 |
Lod Score | 4 | 0.0 |
Microsatellite Repeats | 2 | 0.0 |
Adolescent | 5 | 0.0 |
Adult | 4 | 0.0 |
Alleles | 3 | 0.0 |
Case-Control Studies | 2 | 0.0 |
Epilepsies, Myoclonic/diagnosis/genetics | 2 | 100.0 |
Epilepsy, Generalized/diagnosis/*genetics | 3 | 50.0 |
Polymorphism, Genetic | 2 | 0.0 |
Receptors, GABA-B/*genetics | 2 | 18.0 |
Variation (Genetics) | 2 | 0.0 |
Epilepsy, Generalized/*genetics | 2 | 7.0 |
Chromosomes, Human, Pair 6/*genetics | 4 | 2.0 |
HLA-DQ Antigens/genetics | 3 | 1.0 |
Female | 8 | 0.0 |
Male | 7 | 0.0 |
Disease Susceptibility | 2 | 0.0 |
Epilepsy/*genetics | 2 | 6.0 |
Phenotype | 3 | 0.0 |
*Chromosome Mapping | 2 | 0.0 |
Chromosomes, Human, Pair 6 | 2 | 1.0 |
Family Health | 2 | 0.0 |
Genetic Markers | 2 | 0.0 |
In Situ Hybridization, Fluorescence | 2 | 0.0 |
DNA Mutational Analysis | 3 | 0.0 |
Genetic Predisposition to Disease/*genetics | 2 | 0.0 |
