MeSH term
Frequency | Condition_Probility | Chromosomes, Human, Pair 15/*genetics | 3 | 3.0 |
Female | 10 | 0.0 |
Haplotypes | 2 | 0.0 |
Humans | 24 | 0.0 |
Linkage (Genetics) | 6 | 0.0 |
Male | 11 | 0.0 |
Pedigree | 5 | 0.0 |
Promoter Regions (Genetics)/genetics | 2 | 0.0 |
Receptors, Nicotinic/*genetics | 18 | 30.0 |
Research Support, Non-U.S. Gov't | 18 | 0.0 |
Variation (Genetics) | 2 | 0.0 |
Genetic Predisposition to Disease | 3 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 9 | 0.0 |
*Chromosomes, Human, Pair 15 | 8 | 3.0 |
Family Health | 5 | 0.0 |
*Linkage (Genetics) | 3 | 0.0 |
Schizophrenia, Catatonic/*genetics | 2 | 50.0 |
Adult | 5 | 0.0 |
Base Sequence | 4 | 0.0 |
Child | 3 | 0.0 |
Chromosome Mapping | 4 | 0.0 |
*Gene Duplication | 3 | 2.0 |
Molecular Sequence Data | 4 | 0.0 |
Polymorphism, Genetic | 4 | 0.0 |
Adolescent | 2 | 0.0 |
Alleles | 3 | 0.0 |
Child, Preschool | 2 | 0.0 |
Chromosomes, Human, Pair 15/genetics | 3 | 4.0 |
DNA/genetics | 4 | 0.0 |
Gene Frequency | 2 | 0.0 |
Genotype | 4 | 0.0 |
*Linkage Disequilibrium | 2 | 1.0 |
Microsatellite Repeats | 3 | 0.0 |
Schizophrenia/*genetics | 7 | 3.0 |
Lod Score | 2 | 0.0 |
Middle Aged | 3 | 0.0 |
Receptors, Nicotinic/genetics | 3 | 23.0 |
Research Support, U.S. Gov't, Non-P.H.S. | 4 | 0.0 |
Genetic Markers | 2 | 0.0 |
Linkage (Genetics)/*genetics | 2 | 0.0 |
*Genetic Predisposition to Disease | 2 | 0.0 |
Risk Factors | 2 | 0.0 |
Chromosomes, Human, Pair 15 | 2 | 1.0 |
Sequence Analysis, DNA | 4 | 0.0 |
Phenotype | 2 | 0.0 |
Cloning, Molecular | 2 | 0.0 |
Exons/genetics | 3 | 0.0 |
Introns/genetics | 2 | 0.0 |
Animals | 2 | 0.0 |
Comparative Study | 3 | 0.0 |
Sequence Homology, Nucleic Acid | 2 | 0.0 |
