MeSH term
Frequency | Condition_Probility | Adolescent | 2 | 0.0 |
Amino Acid Sequence | 2 | 0.0 |
Base Sequence | 3 | 0.0 |
Child | 2 | 0.0 |
Child, Preschool | 3 | 0.0 |
DNA Mutational Analysis | 2 | 0.0 |
Female | 6 | 0.0 |
Genes, Dominant | 3 | 0.0 |
Humans | 9 | 0.0 |
Male | 7 | 0.0 |
Molecular Sequence Data | 3 | 0.0 |
*Mutation | 2 | 0.0 |
Pedigree | 5 | 0.0 |
Polymerase Chain Reaction | 3 | 0.0 |
Research Support, Non-U.S. Gov't | 7 | 0.0 |
Adult | 2 | 0.0 |
Cataract/*genetics/pathology | 2 | 25.0 |
*Chromosome Mapping | 3 | 0.0 |
Chromosomes, Human, Pair 22/*genetics | 2 | 2.0 |
Crystallins/*genetics | 6 | 20.0 |
*Genetic Heterogeneity | 2 | 1.0 |
Genotype | 2 | 0.0 |
Infant | 2 | 0.0 |
Linkage (Genetics) | 4 | 0.0 |
Chromosome Mapping | 3 | 0.0 |
*Chromosomes, Human, Pair 22 | 3 | 1.0 |
Research Support, U.S. Gov't, P.H.S. | 4 | 0.0 |
Animals | 3 | 0.0 |
Crosses, Genetic | 2 | 0.0 |
Hybrid Cells | 2 | 0.0 |
Mice, Inbred C57BL | 2 | 0.0 |
Comparative Study | 2 | 0.0 |
Sequence Homology, Nucleic Acid | 2 | 0.0 |
Chromosome Disorders | 2 | 0.0 |
Genetic Markers/*genetics | 2 | 1.0 |
Lod Score | 2 | 0.0 |
Microsatellite Repeats | 2 | 0.0 |
