MeSH term
Frequency | Condition_Probility | Eye Proteins/genetics | 2 | 4.0 |
Genotype | 5 | 0.0 |
Humans | 16 | 0.0 |
Research Support, Non-U.S. Gov't | 13 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 3 | 0.0 |
Adolescent | 5 | 0.0 |
Adult | 9 | 0.0 |
Aged | 5 | 0.0 |
DNA Mutational Analysis | 8 | 0.0 |
Electroretinography | 6 | 3.0 |
Female | 13 | 0.0 |
Genes, Dominant | 3 | 0.0 |
Guanylate Cyclase/*genetics | 9 | 36.0 |
Male | 11 | 0.0 |
Middle Aged | 6 | 0.0 |
*Mutation | 5 | 0.0 |
Pedigree | 10 | 0.0 |
Phenotype | 6 | 0.0 |
Photoreceptors, Vertebrate/*pathology | 3 | 18.0 |
Retinal Degeneration/diagnosis/enzymology/*genetics | 2 | 66.0 |
Visual Acuity | 4 | 2.0 |
Visual Fields | 4 | 6.0 |
Amino Acid Sequence | 2 | 0.0 |
Base Sequence | 3 | 0.0 |
Genes, Dominant/*genetics | 2 | 2.0 |
Heterozygote | 2 | 0.0 |
Mutation/*genetics | 3 | 0.0 |
Polymorphism, Single Nucleotide/genetics | 2 | 0.0 |
Child | 6 | 0.0 |
Chromosomes, Human, Pair 17/genetics | 2 | 1.0 |
Linkage (Genetics) | 2 | 0.0 |
*Mutation, Missense | 2 | 0.0 |
Polymerase Chain Reaction | 2 | 0.0 |
Child, Preschool | 2 | 0.0 |
Eye Proteins/*genetics | 2 | 1.0 |
Infant | 2 | 0.0 |
Polymorphism, Single-Stranded Conformational | 3 | 0.0 |
Proteins/*genetics | 2 | 0.0 |
Aged, 80 and over | 2 | 0.0 |
Prospective Studies | 2 | 0.0 |
Homozygote | 2 | 0.0 |
Molecular Sequence Data | 2 | 0.0 |
Fluorescein Angiography | 2 | 1.0 |
*Chromosome Mapping | 2 | 0.0 |
Guanylate Cyclase/genetics | 2 | 50.0 |
Blindness/congenital/*genetics | 2 | 28.0 |
Mutation/genetics | 2 | 0.0 |
Optic Atrophy, Hereditary, Leber/*genetics | 2 | 18.0 |
