MeSH term
Frequency | Condition_Probility | Abnormalities, Multiple/*genetics | 2 | 0.0 |
Alleles | 4 | 0.0 |
Bardet-Biedl Syndrome/*genetics | 13 | 54.0 |
Base Sequence | 2 | 0.0 |
DNA/genetics | 2 | 0.0 |
DNA Mutational Analysis | 2 | 0.0 |
Female | 14 | 0.0 |
Humans | 22 | 0.0 |
Male | 14 | 0.0 |
Molecular Chaperones/*genetics | 2 | 9.0 |
*Mutation | 3 | 0.0 |
Polydactyly/*genetics | 2 | 9.0 |
Syndrome | 4 | 0.0 |
Amino Acid Sequence | 5 | 0.0 |
Cohort Studies | 4 | 0.0 |
Conserved Sequence | 2 | 0.0 |
Evolution, Molecular | 2 | 0.0 |
Genes, Recessive | 4 | 0.0 |
Genotype | 3 | 0.0 |
Molecular Sequence Data | 8 | 0.0 |
Pedigree | 13 | 0.0 |
Phenotype | 4 | 0.0 |
Proteins/*genetics | 4 | 0.0 |
Research Support, Non-U.S. Gov't | 19 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 11 | 0.0 |
Sequence Homology, Amino Acid | 3 | 0.0 |
Animals | 5 | 0.0 |
Chromosome Mapping | 7 | 0.0 |
Chromosomes, Human, Pair 16/*genetics | 3 | 3.0 |
Comparative Study | 2 | 0.0 |
Mice | 4 | 0.0 |
Rats | 2 | 0.0 |
*Alleles | 2 | 0.0 |
Haplotypes | 3 | 0.0 |
Microsatellite Repeats | 2 | 0.0 |
Mutation | 6 | 0.0 |
Open Reading Frames | 2 | 0.0 |
Cloning, Molecular | 3 | 0.0 |
Consanguinity | 4 | 1.0 |
Genetic Screening | 2 | 0.0 |
*Chromosome Mapping | 2 | 0.0 |
Chromosomes, Human, Pair 15 | 2 | 1.0 |
Chromosomes, Human, Pair 16 | 2 | 1.0 |
Chromosomes, Human, Pair 11/*genetics | 2 | 0.0 |
Newfoundland | 2 | 14.0 |
Linkage (Genetics) | 2 | 0.0 |
Laurence-Moon Syndrome/*genetics | 2 | 66.0 |
Disease Models, Animal | 2 | 0.0 |
Proteins/genetics | 2 | 0.0 |
Adult | 2 | 0.0 |
Kidney/abnormalities | 2 | 10.0 |
*Linkage (Genetics) | 2 | 0.0 |
Mental Retardation/genetics | 2 | 1.0 |
Obesity/genetics | 2 | 3.0 |
Retinitis Pigmentosa/genetics | 2 | 8.0 |
Polydactyly/genetics | 2 | 9.0 |
