MeSH term
Frequency | Condition_Probility | Adult | 5 | 0.0 |
Aged | 4 | 0.0 |
Charcot-Marie-Tooth Disease/genetics | 2 | 8.0 |
Child | 4 | 0.0 |
DNA Mutational Analysis | 4 | 0.0 |
Female | 12 | 0.0 |
Genes, Dominant | 3 | 0.0 |
Hereditary Sensory and Autonomic Neuropathies/genetics | 2 | 100.0 |
Humans | 19 | 0.0 |
Italy | 2 | 0.0 |
Linkage (Genetics) | 6 | 0.0 |
Male | 12 | 0.0 |
Pedigree | 12 | 0.0 |
Research Support, Non-U.S. Gov't | 16 | 0.0 |
Electrophysiology | 2 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 5 | 0.0 |
Charcot-Marie-Tooth Disease/*genetics | 7 | 5.0 |
Genotype | 5 | 0.0 |
Phenotype | 5 | 0.0 |
Charcot-Marie-Tooth Disease/*genetics/*physiopathology | 2 | 22.0 |
Linkage (Genetics)/*genetics | 3 | 1.0 |
Amino Acid Sequence | 3 | 0.0 |
Base Sequence | 3 | 0.0 |
Chromosome Mapping | 6 | 0.0 |
Lod Score | 4 | 0.0 |
Microsatellite Repeats/genetics | 2 | 0.0 |
Molecular Sequence Data | 4 | 0.0 |
Neurofilament Proteins/*genetics | 2 | 13.0 |
Animals | 3 | 0.0 |
*Chromosomes, Human, Pair 3 | 4 | 1.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
X Chromosome/genetics | 2 | 1.0 |
Middle Aged | 5 | 0.0 |
Biopsy | 2 | 0.0 |
Chromosomes, Human, Pair 1 | 2 | 0.0 |
Family Health | 2 | 0.0 |
Genetic Markers | 3 | 0.0 |
Chromosomes, Human, Pair 17 | 2 | 0.0 |
Point Mutation | 2 | 0.0 |
*Point Mutation | 2 | 0.0 |
Polymerase Chain Reaction | 2 | 0.0 |
Recombination, Genetic | 2 | 0.0 |
