MeSH term
Frequency | Condition_Probility | Autistic Disorder/*genetics | 5 | 8.0 |
Chromosomes, Human, Pair 15/*genetics | 5 | 5.0 |
Genotype | 6 | 0.0 |
Humans | 30 | 0.0 |
Linkage Disequilibrium | 4 | 0.0 |
Polymorphism, Single Nucleotide | 3 | 0.0 |
Receptors, GABA-A/*genetics | 16 | 21.0 |
Research Support, Non-U.S. Gov't | 22 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 17 | 0.0 |
Adolescent | 4 | 0.0 |
Alleles | 11 | 0.0 |
Child | 5 | 0.0 |
DNA/genetics | 2 | 0.0 |
English Abstract | 2 | 0.0 |
Epilepsy, Absence/*genetics | 3 | 17.0 |
Female | 15 | 0.0 |
Gene Frequency | 6 | 0.0 |
*Linkage Disequilibrium | 3 | 1.0 |
Male | 18 | 0.0 |
Microsatellite Repeats | 2 | 0.0 |
Receptors, GABA-B/*genetics | 3 | 27.0 |
Base Sequence | 10 | 0.0 |
Chromosome Mapping | 11 | 0.0 |
Family Health | 2 | 0.0 |
Protein Subunits/genetics | 2 | 7.0 |
Linkage (Genetics)/*genetics | 2 | 0.0 |
Microsatellite Repeats/genetics | 2 | 0.0 |
Pedigree | 4 | 0.0 |
Angelman Syndrome/*genetics | 5 | 10.0 |
Chromosome Deletion | 3 | 0.0 |
Chromosomes, Human, Pair 15/genetics | 4 | 5.0 |
Molecular Sequence Data | 10 | 0.0 |
Protein Subunits | 2 | 0.0 |
Receptors, GABA-A/genetics | 3 | 23.0 |
Sequence Deletion | 3 | 0.0 |
Ubiquitin-Protein Ligases | 2 | 0.0 |
Blotting, Southern | 2 | 0.0 |
In Situ Hybridization, Fluorescence | 5 | 0.0 |
Polymerase Chain Reaction | 5 | 0.0 |
Prader-Willi Syndrome/*genetics | 5 | 6.0 |
Polymorphism, Genetic | 3 | 0.0 |
Electrophoresis, Gel, Pulsed-Field | 2 | 0.0 |
Genetic Markers | 8 | 0.0 |
Restriction Mapping | 2 | 0.0 |
*Chromosomes, Human, Pair 15 | 10 | 4.0 |
*Multigene Family | 6 | 0.0 |
Repetitive Sequences, Nucleic Acid | 2 | 0.0 |
Adult | 6 | 0.0 |
Animals | 5 | 0.0 |
Gene Expression Regulation | 2 | 0.0 |
Hybrid Cells | 2 | 0.0 |
Mice | 4 | 0.0 |
Prader-Willi Syndrome/genetics | 2 | 9.0 |
Exons | 2 | 0.0 |
Transcription, Genetic | 2 | 0.0 |
Chromosomes, Human, Pair 15 | 5 | 3.0 |
Cloning, Molecular | 2 | 0.0 |
Protein Conformation | 2 | 0.0 |
Receptors, GABA-A/chemistry/*genetics | 2 | 28.0 |
Genomic Imprinting | 2 | 1.0 |
Comparative Study | 3 | 0.0 |
*Genes, Structural | 2 | 0.0 |
*Polymorphism, Genetic | 3 | 0.0 |
*Repetitive Sequences, Nucleic Acid | 2 | 0.0 |
Phenotype | 3 | 0.0 |
Homozygote | 2 | 0.0 |
Mice, Mutant Strains | 2 | 0.0 |
Research Support, U.S. Gov't, Non-P.H.S. | 3 | 0.0 |
Cell Line | 2 | 0.0 |
