MeSH term
Frequency | Condition_Probility | Base Sequence | 4 | 0.0 |
Chromosomes, Human, Pair 13/*genetics | 3 | 4.0 |
Heparan Sulfate Proteoglycan/*genetics | 5 | 35.0 |
Humans | 7 | 0.0 |
Molecular Sequence Data | 5 | 0.0 |
Research Support, Non-U.S. Gov't | 6 | 0.0 |
Amino Acid Sequence | 4 | 0.0 |
Blotting, Northern | 2 | 0.0 |
In Situ Hybridization, Fluorescence | 2 | 0.0 |
Chromosome Mapping | 2 | 0.0 |
*Chromosomes, Human, Pair 13 | 2 | 1.0 |
DNA, Complementary | 2 | 0.0 |
Heparitin Sulfate/*genetics | 2 | 10.0 |
Proteoglycans/*genetics | 2 | 3.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
Cell Line, Tumor | 2 | 0.0 |
