MeSH term
Frequency | Condition_Probility | Autistic Disorder/*genetics | 4 | 6.0 |
Chromosomes, Human, Pair 15/*genetics | 5 | 5.0 |
Genotype | 3 | 0.0 |
Humans | 9 | 0.0 |
Polymorphism, Single Nucleotide | 3 | 0.0 |
Receptors, GABA-A/*genetics | 4 | 5.0 |
Research Support, Non-U.S. Gov't | 6 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 6 | 0.0 |
Alleles | 2 | 0.0 |
Base Sequence | 4 | 0.0 |
Chromosome Mapping | 4 | 0.0 |
Family Health | 2 | 0.0 |
Female | 5 | 0.0 |
Gene Frequency | 2 | 0.0 |
*Linkage Disequilibrium | 2 | 1.0 |
Male | 5 | 0.0 |
Chromosome Deletion | 2 | 0.0 |
Chromosomes, Human, Pair 15/genetics | 2 | 2.0 |
Molecular Sequence Data | 3 | 0.0 |
Sequence Deletion | 2 | 0.0 |
Ubiquitin-Protein Ligases | 2 | 0.0 |
Genetic Markers | 2 | 0.0 |
Adult | 2 | 0.0 |
Animals | 3 | 0.0 |
Mice | 3 | 0.0 |
Cloning, Molecular | 2 | 0.0 |
Protein Conformation | 2 | 0.0 |
Receptors, GABA-A/chemistry/*genetics | 2 | 28.0 |
Adolescent | 2 | 0.0 |
Child | 2 | 0.0 |
Phenotype | 3 | 0.0 |
