MeSH term
Frequency | Condition_Probility | Adolescent | 2 | 0.0 |
Adult | 3 | 0.0 |
Amino Acid Sequence | 8 | 0.0 |
Cadherins/*genetics | 9 | 9.0 |
DNA Mutational Analysis | 6 | 0.0 |
Deafness/*genetics | 4 | 3.0 |
Female | 7 | 0.0 |
Humans | 14 | 0.0 |
Male | 7 | 0.0 |
Molecular Sequence Data | 6 | 0.0 |
*Mutation | 3 | 0.0 |
Phenotype | 7 | 0.0 |
Research Support, Non-U.S. Gov't | 15 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 10 | 0.0 |
Retinitis Pigmentosa/*genetics | 6 | 4.0 |
Syndrome | 9 | 0.0 |
Exons/genetics | 3 | 0.0 |
Hearing Loss, Sensorineural/*genetics | 6 | 6.0 |
Middle Aged | 2 | 0.0 |
Mutation/*genetics | 5 | 0.0 |
Pedigree | 5 | 0.0 |
Polymorphism, Single-Stranded Conformational | 2 | 0.0 |
*Alleles | 2 | 0.0 |
Animals | 16 | 0.0 |
Base Sequence | 6 | 0.0 |
Binding Sites | 2 | 0.0 |
Mice | 13 | 0.0 |
Mice, Inbred BALB C | 2 | 0.0 |
Mice, Inbred C57BL | 4 | 0.0 |
Mice, Inbred CBA | 5 | 1.0 |
Mice, Inbred Strains | 3 | 0.0 |
Mutation | 3 | 0.0 |
Consanguinity | 2 | 0.0 |
Genotype | 5 | 0.0 |
Vestibular Diseases/*genetics | 2 | 50.0 |
Hearing Loss, Sensorineural/*genetics/pathology | 2 | 20.0 |
Alleles | 5 | 0.0 |
Chromosome Mapping | 5 | 0.0 |
Cloning, Molecular | 3 | 0.0 |
In Situ Hybridization | 2 | 0.0 |
Membrane Proteins/genetics | 2 | 0.0 |
Mice, Mutant Strains | 3 | 0.0 |
Reverse Transcriptase Polymerase Chain Reaction | 3 | 0.0 |
Disease Models, Animal | 2 | 0.0 |
Homozygote | 3 | 0.0 |
Cadherins/chemistry/*genetics/metabolism | 2 | 100.0 |
RNA, Messenger/analysis/genetics | 3 | 0.0 |
Hearing/physiology | 2 | 28.0 |
Microscopy, Electron, Scanning | 3 | 1.0 |
Hair Cells/*metabolism/ultrastructure | 2 | 100.0 |
Aging | 2 | 0.0 |
Heterozygote | 2 | 0.0 |
Myosins/*genetics | 2 | 3.0 |
Species Specificity | 2 | 0.0 |
Carrier Proteins/*genetics | 2 | 0.0 |
Cadherins/*genetics/physiology | 2 | 33.0 |
