MeSH term
Frequency | Condition_Probility | Humans | 8 | 0.0 |
Research Support, Non-U.S. Gov't | 6 | 0.0 |
Comparative Study | 2 | 0.0 |
*Chromosome Aberrations | 2 | 0.0 |
*Chromosome Disorders | 2 | 2.0 |
Chromosomes, Human, Pair 14/*genetics | 2 | 2.0 |
Chromosomes, Human, Pair 2/*genetics | 2 | 1.0 |
*In Situ Hybridization | 2 | 14.0 |
In Situ Hybridization, Fluorescence | 2 | 0.0 |
Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated/*genetics | 2 | 40.0 |
Tumor Cells, Cultured | 2 | 0.0 |
Animals | 3 | 0.0 |
Amino Acid Sequence | 3 | 0.0 |
Base Sequence | 3 | 0.0 |
Molecular Sequence Data | 3 | 0.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
Chromosome Mapping | 2 | 0.0 |
Transcription Factors/*genetics | 2 | 0.0 |
