MeSH term
Frequency | Condition_Probility | *Chromosomes, Human, Pair 15 | 3 | 1.0 |
Female | 6 | 0.0 |
HLA-DQ Antigens/genetics | 2 | 0.0 |
Humans | 8 | 0.0 |
*Linkage (Genetics) | 2 | 0.0 |
Male | 6 | 0.0 |
Microsatellite Repeats | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 7 | 0.0 |
Animals | 2 | 0.0 |
Chromosome Mapping | 3 | 0.0 |
Crosses, Genetic | 2 | 0.0 |
Rats | 2 | 0.0 |
Adult | 2 | 0.0 |
*Chromosome Mapping | 2 | 0.0 |
Chromosomes, Human, Pair 11 | 3 | 0.0 |
Chromosomes, Human, Pair 15 | 2 | 1.0 |
Genetic Markers | 2 | 0.0 |
Linkage (Genetics) | 3 | 0.0 |
Nuclear Family | 3 | 1.0 |
Diabetes Mellitus, Type 1/*genetics | 4 | 1.0 |
Genetic Predisposition to Disease | 4 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 3 | 0.0 |
Genetic Heterogeneity | 2 | 0.0 |
Lod Score | 2 | 0.0 |
