MeSH term
Frequency | Condition_Probility | Abnormalities, Multiple/*genetics | 3 | 0.0 |
Alleles | 3 | 0.0 |
Bardet-Biedl Syndrome/*genetics | 14 | 58.0 |
Base Sequence | 3 | 0.0 |
DNA/genetics | 3 | 0.0 |
DNA Mutational Analysis | 4 | 0.0 |
Female | 15 | 0.0 |
Humans | 27 | 0.0 |
Male | 14 | 0.0 |
Molecular Chaperones/*genetics | 2 | 9.0 |
*Mutation | 4 | 0.0 |
Polydactyly/*genetics | 2 | 9.0 |
Syndrome | 6 | 0.0 |
Amino Acid Sequence | 4 | 0.0 |
Cohort Studies | 3 | 0.0 |
Conserved Sequence | 2 | 0.0 |
Genes, Recessive | 3 | 0.0 |
Genotype | 5 | 0.0 |
Molecular Sequence Data | 10 | 0.0 |
Pedigree | 14 | 0.0 |
Phenotype | 3 | 0.0 |
Proteins/*genetics | 5 | 0.0 |
Research Support, Non-U.S. Gov't | 21 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 10 | 0.0 |
Sequence Homology, Amino Acid | 3 | 0.0 |
Animals | 3 | 0.0 |
Mice | 2 | 0.0 |
Proteins/*genetics/metabolism | 2 | 0.0 |
Cloning, Molecular | 2 | 0.0 |
Consanguinity | 5 | 1.0 |
Expressed Sequence Tags | 2 | 0.0 |
Mutation | 5 | 0.0 |
Obesity/*genetics | 2 | 1.0 |
Adult | 5 | 0.0 |
Chromosome Mapping | 8 | 0.0 |
Middle Aged | 4 | 0.0 |
Family Health | 2 | 0.0 |
Lod Score | 3 | 0.0 |
Mental Retardation/genetics | 3 | 2.0 |
Microsatellite Repeats | 3 | 0.0 |
Obesity/genetics | 4 | 7.0 |
Polydactyly/genetics | 4 | 19.0 |
Retinitis Pigmentosa/genetics | 3 | 12.0 |
*Chromosome Mapping | 3 | 0.0 |
Chromosomes, Human, Pair 11/*genetics | 5 | 2.0 |
Neoplasm Proteins/genetics | 2 | 0.0 |
Newfoundland | 3 | 21.0 |
*Proto-Oncogene Proteins | 2 | 0.0 |
Mutation/genetics | 2 | 0.0 |
Exons | 2 | 0.0 |
Polymorphism, Single-Stranded Conformational | 2 | 0.0 |
Sequence Analysis, DNA | 2 | 0.0 |
Spinocerebellar Degenerations/genetics | 2 | 40.0 |
Founder Effect | 2 | 1.0 |
Haplotypes | 2 | 0.0 |
Linkage (Genetics) | 2 | 0.0 |
Proteins/genetics | 3 | 0.0 |
Kidney/abnormalities | 2 | 10.0 |
*Linkage (Genetics) | 2 | 0.0 |
*Chromosomes, Human, Pair 11 | 2 | 0.0 |
Genetic Markers | 2 | 0.0 |
Hypogonadism/genetics | 2 | 25.0 |
