MeSH term
Frequency | Condition_Probility | Animals | 6 | 0.0 |
Base Sequence | 5 | 0.0 |
Comparative Study | 4 | 0.0 |
Exons | 2 | 0.0 |
Humans | 31 | 0.0 |
Mice | 3 | 0.0 |
Molecular Sequence Data | 6 | 0.0 |
Rats | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 24 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 15 | 0.0 |
Species Specificity | 2 | 0.0 |
Tissue Distribution | 2 | 0.0 |
Collagen/*genetics | 12 | 2.0 |
Exons/genetics | 2 | 0.0 |
Polymorphism, Genetic/*genetics | 2 | 0.0 |
*Chromosome Mapping | 2 | 0.0 |
Cohort Studies | 2 | 0.0 |
*Linkage (Genetics) | 6 | 0.0 |
Lod Score | 2 | 0.0 |
Microsatellite Repeats | 3 | 0.0 |
Myopia/*genetics | 2 | 20.0 |
Child | 6 | 0.0 |
Chromosome Mapping | 2 | 0.0 |
Connective Tissue Diseases/*genetics/pathology | 4 | 80.0 |
DNA Mutational Analysis | 3 | 0.0 |
Female | 15 | 0.0 |
Male | 16 | 0.0 |
*Mutation | 5 | 0.0 |
Pedigree | 12 | 0.0 |
Phenotype | 3 | 0.0 |
Syndrome | 11 | 0.0 |
Vitreous Body/*pathology | 2 | 15.0 |
Gene Expression Profiling | 2 | 0.0 |
Gene Expression Regulation, Neoplastic | 2 | 0.0 |
Abnormalities, Multiple/*genetics | 2 | 0.0 |
Hearing Loss, Sensorineural/*genetics | 2 | 2.0 |
Prospective Studies | 3 | 0.0 |
Abnormalities, Multiple/*genetics/pathology | 3 | 4.0 |
Ear/abnormalities | 2 | 20.0 |
Eye Diseases, Hereditary/genetics/pathology | 3 | 100.0 |
Face/abnormalities | 3 | 4.0 |
Joints/abnormalities | 3 | 100.0 |
Mutation | 3 | 0.0 |
Child, Preschool | 3 | 0.0 |
Adult | 6 | 0.0 |
Tumor Cells, Cultured | 2 | 0.0 |
Aged | 4 | 0.0 |
Middle Aged | 3 | 0.0 |
Chromosomes, Human, Pair 19 | 2 | 1.0 |
Genetic Markers | 2 | 0.0 |
Mutation/genetics | 2 | 0.0 |
Linkage (Genetics) | 2 | 0.0 |
Cloning, Molecular | 2 | 0.0 |
*Genes, Structural | 2 | 0.0 |
Collagen Type XI/*genetics | 2 | 40.0 |
Proteoglycans/genetics | 2 | 8.0 |
Collagen Type XI/genetics | 2 | 66.0 |
Eye Diseases, Hereditary/*diagnosis/genetics | 2 | 100.0 |
Infant, Newborn | 2 | 0.0 |
*Chromosomes, Human, Pair 1 | 2 | 0.0 |
