MeSH term
Frequency | Condition_Probility | Base Sequence | 7 | 0.0 |
Blood Platelets/pathology | 3 | 16.0 |
DNA Mutational Analysis | 6 | 0.0 |
Humans | 23 | 0.0 |
Inclusion Bodies/pathology | 4 | 19.0 |
Infant | 2 | 0.0 |
Male | 11 | 0.0 |
Molecular Motors/*genetics | 2 | 100.0 |
Myosin Heavy Chains/*genetics | 9 | 22.0 |
Research Support, Non-U.S. Gov't | 13 | 0.0 |
Thrombocytopenia/blood/*genetics | 2 | 33.0 |
Adult | 4 | 0.0 |
Diagnosis, Differential | 2 | 0.0 |
Pedigree | 5 | 0.0 |
Amino Acid Sequence | 5 | 0.0 |
Animals | 5 | 0.0 |
Blood Platelet Disorders/*genetics/pathology | 2 | 100.0 |
DNA, Complementary/chemistry/genetics | 2 | 0.0 |
Gene Expression | 2 | 0.0 |
Mice | 2 | 0.0 |
*Molecular Motors | 9 | 60.0 |
Molecular Sequence Data | 7 | 0.0 |
Sequence Analysis, DNA | 2 | 0.0 |
Syndrome | 8 | 0.0 |
Deafness/genetics | 2 | 4.0 |
Female | 8 | 0.0 |
Genes, Dominant | 6 | 0.0 |
*Mutation | 7 | 0.0 |
Thrombocytopenia/genetics | 2 | 100.0 |
Blood Platelets/*pathology | 2 | 13.0 |
DNA Primers/genetics | 2 | 0.0 |
Genotype | 5 | 0.0 |
Leukocytes/*pathology | 4 | 25.0 |
Phenotype | 4 | 0.0 |
Adolescent | 3 | 0.0 |
Aged | 2 | 0.0 |
Hearing Loss, Sensorineural/*genetics | 2 | 2.0 |
Middle Aged | 3 | 0.0 |
Protein Isoforms/genetics | 2 | 0.0 |
Thrombocytopenia/*genetics | 3 | 23.0 |
Genetic Markers | 2 | 0.0 |
Leukocytes/pathology | 2 | 6.0 |
Microscopy, Electron | 2 | 0.0 |
Molecular Motors/genetics | 2 | 40.0 |
Research Support, U.S. Gov't, P.H.S. | 4 | 0.0 |
Alleles | 2 | 0.0 |
Chromosomes, Human, Pair 22 | 2 | 1.0 |
Family Health | 3 | 0.0 |
Myosin Heavy Chains/chemistry/*genetics | 2 | 33.0 |
Protein Structure, Tertiary | 2 | 0.0 |
Sequence Homology, Amino Acid | 3 | 0.0 |
Models, Molecular | 3 | 0.0 |
Protein Conformation | 2 | 0.0 |
Microscopy, Fluorescence | 2 | 0.0 |
Mutation | 4 | 0.0 |
English Abstract | 3 | 0.0 |
Myosin Heavy Chains/genetics | 2 | 9.0 |
