MeSH term
Frequency | Condition_Probility | Humans | 22 | 0.0 |
Adolescent | 2 | 0.0 |
Adult | 2 | 0.0 |
Biopsy | 3 | 0.0 |
Child | 2 | 0.0 |
Child, Preschool | 2 | 0.0 |
DNA Mutational Analysis | 5 | 0.0 |
Female | 4 | 0.0 |
Infant | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 17 | 0.0 |
Amino Acid Sequence | 5 | 0.0 |
Base Sequence | 7 | 0.0 |
Cells, Cultured | 3 | 0.0 |
Genetic Markers | 2 | 0.0 |
Molecular Sequence Data | 8 | 0.0 |
Proteins/*genetics | 2 | 0.0 |
Sequence Tagged Sites | 2 | 0.0 |
Phenotype | 2 | 0.0 |
Animals | 6 | 0.0 |
*Drosophila Proteins | 3 | 0.0 |
Organ Specificity | 2 | 0.0 |
Male | 5 | 0.0 |
Tropomyosin/*genetics | 8 | 44.0 |
Chromosome Mapping | 3 | 0.0 |
*Chromosomes, Human, Pair 1 | 3 | 0.0 |
DNA Primers | 2 | 0.0 |
Karyotyping | 2 | 0.0 |
Protein-Tyrosine Kinase/*genetics | 2 | 0.0 |
3T3 Cells | 2 | 0.0 |
Mice | 3 | 0.0 |
Proto-Oncogene Proteins/*genetics | 2 | 0.0 |
Receptor Protein-Tyrosine Kinases/*genetics | 2 | 0.0 |
Receptor, trkA | 3 | 5.0 |
Receptors, Nerve Growth Factor/*genetics | 2 | 6.0 |
Linkage (Genetics) | 2 | 0.0 |
Exons | 4 | 0.0 |
English Abstract | 2 | 0.0 |
Mutation | 2 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 3 | 0.0 |
Mutation, Missense | 2 | 0.0 |
