MeSH term
Frequency | Condition_Probility | Acute Disease | 4 | 0.0 |
Adult | 6 | 0.0 |
Aged | 5 | 0.0 |
*Chromosomal Proteins, Non-Histone | 2 | 0.0 |
Female | 10 | 0.0 |
Humans | 22 | 0.0 |
Leukemia, Myeloid/*genetics | 2 | 1.0 |
Male | 8 | 0.0 |
Middle Aged | 5 | 0.0 |
Research Support, Non-U.S. Gov't | 17 | 0.0 |
Translocation, Genetic | 2 | 0.0 |
Research Support, U.S. Gov't, Non-P.H.S. | 2 | 0.0 |
Karyotyping | 3 | 0.0 |
Syndrome | 2 | 0.0 |
*Translocation, Genetic | 2 | 0.0 |
*Chromosomes, Human, Pair 5 | 8 | 3.0 |
Genetic Predisposition to Disease | 2 | 0.0 |
Linkage (Genetics) | 3 | 0.0 |
Pedigree | 5 | 0.0 |
Cell Line | 3 | 0.0 |
Mutation | 2 | 0.0 |
Transfection | 5 | 0.0 |
*Chromosome Deletion | 4 | 0.0 |
Chromosome Mapping | 8 | 0.0 |
Chromosomes, Human, Pair 5/*genetics | 2 | 2.0 |
Genetic Markers | 5 | 0.0 |
Animals | 9 | 0.0 |
Comparative Study | 5 | 0.0 |
Mice | 7 | 0.0 |
Rats | 2 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 10 | 0.0 |
Base Sequence | 4 | 0.0 |
Cloning, Molecular | 2 | 0.0 |
Molecular Sequence Data | 4 | 0.0 |
Mutagenesis, Site-Directed | 2 | 0.0 |
Alleles | 3 | 0.0 |
Polymorphism, Restriction Fragment Length | 2 | 0.0 |
Blotting, Southern | 2 | 0.0 |
*Chromosome Mapping | 3 | 0.0 |
DNA Probes | 2 | 0.0 |
Hamsters | 3 | 0.0 |
Hybrid Cells | 3 | 0.0 |
Nucleic Acid Hybridization | 2 | 0.0 |