MeSH term
Frequency | Condition_Probility | Abnormalities, Multiple/*genetics | 2 | 0.0 |
Alleles | 4 | 0.0 |
Bardet-Biedl Syndrome/*genetics | 10 | 41.0 |
Base Sequence | 3 | 0.0 |
Child, Preschool | 2 | 0.0 |
DNA/genetics | 3 | 0.0 |
DNA Mutational Analysis | 3 | 0.0 |
Female | 13 | 0.0 |
Humans | 23 | 0.0 |
Male | 13 | 0.0 |
*Mutation | 4 | 0.0 |
Polydactyly/*genetics | 2 | 9.0 |
Syndrome | 4 | 0.0 |
Amino Acid Sequence | 4 | 0.0 |
Cohort Studies | 2 | 0.0 |
Conserved Sequence | 3 | 0.0 |
Genes, Recessive | 3 | 0.0 |
Genotype | 4 | 0.0 |
Molecular Sequence Data | 9 | 0.0 |
Pedigree | 10 | 0.0 |
Phenotype | 7 | 0.0 |
Proteins/*genetics | 3 | 0.0 |
Research Support, Non-U.S. Gov't | 18 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 8 | 0.0 |
Sequence Homology, Amino Acid | 5 | 0.0 |
Animals | 8 | 0.0 |
Mice | 6 | 0.0 |
Proteins/*genetics/metabolism | 2 | 0.0 |
Cloning, Molecular | 3 | 0.0 |
Consanguinity | 3 | 0.0 |
Expressed Sequence Tags | 2 | 0.0 |
Mutation | 3 | 0.0 |
Chromosome Mapping | 6 | 0.0 |
Genetic Markers | 2 | 0.0 |
Linkage (Genetics) | 4 | 0.0 |
Adolescent | 2 | 0.0 |
Adult | 4 | 0.0 |
Exons/genetics | 2 | 0.0 |
Gene Frequency | 2 | 0.0 |
Chromosomes, Human, Pair 11/*genetics | 2 | 0.0 |
Eye Proteins/genetics | 2 | 4.0 |
Newfoundland | 2 | 14.0 |
Blotting, Northern | 2 | 0.0 |
In Situ Hybridization | 2 | 0.0 |
Retina/metabolism | 2 | 3.0 |
Tissue Distribution | 2 | 0.0 |
Chromosomes, Human, Pair 15/*genetics | 2 | 2.0 |
Exons | 2 | 0.0 |
Gene Expression Regulation, Developmental | 2 | 0.0 |
Laurence-Moon Syndrome/*genetics | 2 | 66.0 |
Mice, Inbred C57BL | 2 | 0.0 |
Polymorphism, Single-Stranded Conformational | 2 | 0.0 |
Apoptosis | 2 | 0.0 |
Obesity/genetics | 3 | 5.0 |
Haplotypes | 2 | 0.0 |
Proteins/genetics | 2 | 0.0 |
Kidney/abnormalities | 2 | 10.0 |
*Linkage (Genetics) | 2 | 0.0 |
Mental Retardation/genetics | 2 | 1.0 |
Retinitis Pigmentosa/genetics | 2 | 8.0 |
Polydactyly/genetics | 2 | 9.0 |
