MeSH term
Frequency | Condition_Probility | Base Sequence | 3 | 0.0 |
Chromosomes, Human, Pair 11/*genetics | 2 | 0.0 |
Diabetes Mellitus, Type 1/*genetics | 15 | 7.0 |
Female | 6 | 0.0 |
Humans | 21 | 0.0 |
Male | 6 | 0.0 |
Microsatellite Repeats | 4 | 0.0 |
Molecular Sequence Data | 3 | 0.0 |
Research Support, Non-U.S. Gov't | 18 | 0.0 |
Sequence Analysis, DNA | 2 | 0.0 |
Animals | 6 | 0.0 |
Chromosome Mapping | 10 | 0.0 |
Comparative Study | 2 | 0.0 |
Crosses, Genetic | 2 | 0.0 |
*Chromosomes, Human, Pair 11 | 3 | 0.0 |
Genetic Markers | 3 | 0.0 |
Genetic Predisposition to Disease | 6 | 0.0 |
Genotype | 5 | 0.0 |
*Linkage Disequilibrium | 2 | 1.0 |
Research Support, U.S. Gov't, P.H.S. | 8 | 0.0 |
Adolescent | 2 | 0.0 |
Adult | 5 | 0.0 |
Alleles | 2 | 0.0 |
Child | 2 | 0.0 |
Chromosomes, Human, Pair 11 | 5 | 1.0 |
Linkage (Genetics) | 5 | 0.0 |
Research Support, U.S. Gov't, Non-P.H.S. | 2 | 0.0 |
Mutation | 2 | 0.0 |
Lod Score | 4 | 0.0 |
Nuclear Family | 3 | 1.0 |
Diabetes Mellitus, Type 1/genetics | 2 | 5.0 |
Genome, Human | 2 | 0.0 |
Mice | 2 | 0.0 |
*Linkage (Genetics) | 3 | 0.0 |
*Chromosome Mapping | 3 | 0.0 |
Genetic Heterogeneity | 2 | 0.0 |
