MeSH term
Frequency | Condition_Probility | Amino Acid Sequence | 9 | 0.0 |
Animals | 12 | 0.0 |
Collagen Type XI/*genetics | 4 | 80.0 |
Mice | 9 | 0.0 |
Molecular Sequence Data | 13 | 0.0 |
Promoter Regions (Genetics) | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 35 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 18 | 0.0 |
Sequence Homology, Amino Acid | 3 | 0.0 |
Abnormalities, Multiple/*genetics/pathology | 4 | 5.0 |
Base Sequence | 12 | 0.0 |
Child, Preschool | 7 | 0.0 |
DNA Mutational Analysis | 4 | 0.0 |
Face/abnormalities | 3 | 4.0 |
Female | 24 | 0.0 |
Humans | 44 | 0.0 |
Male | 25 | 0.0 |
Pedigree | 17 | 0.0 |
Syndrome | 13 | 0.0 |
Alleles | 3 | 0.0 |
Heterozygote | 2 | 0.0 |
Mice, Inbred C57BL | 2 | 0.0 |
Collagen/*genetics | 19 | 4.0 |
Comparative Study | 3 | 0.0 |
Mice, Transgenic | 2 | 0.0 |
Microscopy, Electron | 2 | 0.0 |
Phenotype | 4 | 0.0 |
Audiometry, Pure-Tone | 2 | 5.0 |
Cross-Sectional Studies | 3 | 0.0 |
Disease Progression | 3 | 0.0 |
Genes, Dominant | 3 | 0.0 |
Hearing Loss, Sensorineural/diagnosis/*genetics | 2 | 12.0 |
*Linkage (Genetics) | 6 | 0.0 |
Mutation | 7 | 0.0 |
Adolescent | 5 | 0.0 |
Adult | 11 | 0.0 |
Aged | 6 | 0.0 |
Child | 6 | 0.0 |
Infant | 4 | 0.0 |
Middle Aged | 9 | 0.0 |
Alternative Splicing | 2 | 0.0 |
Cells, Cultured | 3 | 0.0 |
Exons | 5 | 0.0 |
Introns | 2 | 0.0 |
Linkage Disequilibrium | 2 | 0.0 |
Spine/*pathology | 2 | 50.0 |
Chromosome Mapping | 9 | 0.0 |
Chromosomes, Human, Pair 6 | 4 | 2.0 |
Ossification of Posterior Longitudinal Ligament/*genetics | 3 | 75.0 |
Cloning, Molecular | 2 | 0.0 |
Japan | 3 | 0.0 |
Linkage (Genetics)/genetics | 3 | 1.0 |
Major Histocompatibility Complex/*genetics | 5 | 3.0 |
Phylogeny | 2 | 0.0 |
Analysis of Variance | 2 | 0.0 |
Chromosome Disorders | 2 | 0.0 |
Linear Models | 2 | 0.0 |
DNA Primers | 3 | 0.0 |
Polymerase Chain Reaction | 2 | 0.0 |
Procollagen/*genetics | 4 | 3.0 |
Exons/genetics | 3 | 0.0 |
*Mutation | 5 | 0.0 |
Mutation/*genetics | 3 | 0.0 |
Connective Tissue Diseases/*genetics | 3 | 37.0 |
Hearing Loss, Sensorineural/*genetics | 2 | 2.0 |
Prevalence | 2 | 0.0 |
DNA/genetics | 2 | 0.0 |
Connective Tissue Diseases/*genetics/pathology | 2 | 40.0 |
Ear/abnormalities | 2 | 20.0 |
Eye Diseases, Hereditary/genetics/pathology | 2 | 66.0 |
Joints/abnormalities | 2 | 66.0 |
Gene Frequency | 3 | 0.0 |
Haplotypes | 3 | 0.0 |
Receptors, Retinoic Acid/*genetics | 2 | 3.0 |
Retinoid X Receptors | 2 | 0.0 |
Transcription Factors/*genetics | 2 | 0.0 |
Variation (Genetics) | 2 | 0.0 |
Eye Diseases/genetics | 2 | 15.0 |
Sequence Analysis, DNA | 2 | 0.0 |
Chromosomes, Human, Pair 19 | 2 | 1.0 |
Genetic Markers | 2 | 0.0 |
Mutation/genetics | 2 | 0.0 |
Polymorphism, Restriction Fragment Length | 2 | 0.0 |
Collagen/genetics | 2 | 2.0 |
Eye Diseases/*genetics | 2 | 11.0 |
Linkage (Genetics) | 3 | 0.0 |
Sequence Homology, Nucleic Acid | 4 | 0.0 |
Genotype | 2 | 0.0 |
*Chromosome Mapping | 2 | 0.0 |
*Chromosomes, Human, Pair 6 | 5 | 1.0 |
Cosmids | 3 | 0.0 |
DNA | 2 | 0.0 |
Research Support, U.S. Gov't, Non-P.H.S. | 2 | 0.0 |
Blotting, Southern | 3 | 0.0 |
Restriction Mapping | 2 | 0.0 |
Infant, Newborn | 2 | 0.0 |