MeSH term
Frequency | Condition_Probility | Diabetes Mellitus/*genetics | 2 | 6.0 |
Gene Frequency | 7 | 0.0 |
Humans | 35 | 0.0 |
Membrane Proteins/*genetics | 22 | 2.0 |
*Mutation | 6 | 0.0 |
Polymorphism, Genetic | 4 | 0.0 |
Research Support, Non-U.S. Gov't | 24 | 0.0 |
Spain | 4 | 1.0 |
Wolfram Syndrome/genetics | 2 | 100.0 |
Audiometry | 3 | 6.0 |
DNA Mutational Analysis | 9 | 0.0 |
Female | 18 | 0.0 |
Hearing Loss, Sensorineural/*genetics | 2 | 2.0 |
Lod Score | 2 | 0.0 |
Male | 19 | 0.0 |
Microsatellite Repeats/genetics | 2 | 0.0 |
Multigene Family/genetics | 2 | 1.0 |
Mutation/*genetics | 7 | 0.0 |
Pedigree | 10 | 0.0 |
Polymerase Chain Reaction | 3 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 9 | 0.0 |
Adult | 15 | 0.0 |
Alleles | 9 | 0.0 |
DNA/chemistry/genetics | 3 | 0.0 |
Membrane Proteins/genetics | 2 | 0.0 |
Middle Aged | 10 | 0.0 |
Mutation, Missense | 8 | 1.0 |
Point Mutation | 3 | 0.0 |
Polymorphism, Single Nucleotide/genetics | 3 | 1.0 |
Polymorphism, Single-Stranded Conformational | 6 | 0.0 |
*Suicide | 2 | 11.0 |
DNA Primers | 2 | 0.0 |
Diabetes Mellitus, Type 2/*genetics | 2 | 1.0 |
Exons | 5 | 0.0 |
Haplotypes | 4 | 0.0 |
*Variation (Genetics) | 2 | 0.0 |
Connexins/*genetics | 2 | 1.0 |
Amino Acid Sequence | 2 | 0.0 |
Animals | 3 | 0.0 |
Base Sequence | 6 | 0.0 |
Chromosome Mapping | 2 | 0.0 |
Chromosomes, Human, Pair 4/genetics | 3 | 4.0 |
Cloning, Molecular | 3 | 0.0 |
Family Health | 4 | 0.0 |
Hearing Loss, Sensorineural/*genetics/pathology | 2 | 20.0 |
Heterozygote | 2 | 0.0 |
Mice | 2 | 0.0 |
Microsatellite Repeats | 3 | 0.0 |
Molecular Sequence Data | 6 | 0.0 |
Phenotype | 8 | 0.0 |
Auditory Threshold | 2 | 5.0 |
Mutation | 5 | 0.0 |
Polymorphism, Single Nucleotide | 2 | 0.0 |
Mutation/genetics | 2 | 0.0 |
Adolescent | 7 | 0.0 |
Child | 7 | 0.0 |
Genotype | 7 | 0.0 |
Linkage (Genetics) | 2 | 0.0 |
Wolfram Syndrome/*complications/*genetics | 2 | 100.0 |
Child, Preschool | 2 | 0.0 |
Italy | 2 | 0.0 |
Wolfram Syndrome/*genetics | 9 | 90.0 |
Codon, Nonsense | 2 | 1.0 |
DNA, Mitochondrial/genetics | 2 | 4.0 |
Diabetes Mellitus/genetics | 2 | 5.0 |
Gene Deletion | 2 | 0.0 |
Sequence Analysis, DNA | 3 | 0.0 |
Bipolar Disorder/*genetics | 2 | 1.0 |
Chromosomes, Human, Pair 4/*genetics | 2 | 2.0 |
Genetic Predisposition to Disease/genetics | 2 | 0.0 |
Heterozygote Detection | 2 | 0.0 |
Linkage (Genetics)/*genetics | 2 | 0.0 |
Aged | 2 | 0.0 |
Wolfram Syndrome/diagnosis/*genetics | 2 | 100.0 |
Comparative Study | 3 | 0.0 |
Japan | 2 | 0.0 |
Frameshift Mutation | 2 | 0.0 |
Membrane Proteins/chemistry/*genetics | 2 | 3.0 |
Optic Atrophy/genetics | 2 | 66.0 |
*Chromosomes, Human, Pair 4 | 3 | 1.0 |
Schizophrenia/*genetics | 2 | 0.0 |
Age of Onset | 4 | 0.0 |
Longitudinal Studies | 2 | 0.0 |
Alternative Splicing | 2 | 0.0 |
Exons/genetics | 2 | 0.0 |
Wolfram Syndrome/*diagnosis/*genetics | 2 | 100.0 |
Severity of Illness Index | 2 | 0.0 |
