MeSH term
Frequency | Condition_Probility | Animals | 11 | 0.0 |
Chondrodysplasia Punctata/genetics | 2 | 40.0 |
Humans | 20 | 0.0 |
*Mutation | 4 | 0.0 |
Rats | 2 | 0.0 |
Receptors, Cytoplasmic and Nuclear/*genetics | 5 | 6.0 |
Research Support, Non-U.S. Gov't | 10 | 0.0 |
Zellweger Syndrome/genetics | 3 | 33.0 |
Amino Acid Sequence | 8 | 0.0 |
Molecular Sequence Data | 9 | 0.0 |
Peroxisomes/*metabolism | 2 | 7.0 |
Genotype | 4 | 0.0 |
Mutation | 5 | 0.0 |
Phenotype | 5 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 11 | 0.0 |
Chondrodysplasia Punctata, Rhizomelic/*genetics | 6 | 100.0 |
Microbodies/metabolism | 2 | 14.0 |
Receptors, Cytoplasmic and Nuclear/*genetics/metabolism | 2 | 6.0 |
Cells, Cultured | 6 | 0.0 |
Base Sequence | 4 | 0.0 |
Child | 2 | 0.0 |
Female | 2 | 0.0 |
Male | 3 | 0.0 |
Polymerase Chain Reaction | 2 | 0.0 |
Fibroblasts | 4 | 0.0 |
Genetic Complementation Test | 2 | 0.0 |
Peroxisomal Disorders/*genetics | 2 | 10.0 |
Receptors, Cytoplasmic and Nuclear/metabolism | 2 | 1.0 |
Cloning, Molecular | 2 | 0.0 |
Sequence Homology, Amino Acid | 6 | 0.0 |
Chromosome Mapping | 2 | 0.0 |
DNA, Complementary/genetics | 4 | 0.0 |
Gene Expression | 4 | 0.0 |
Homozygote | 2 | 0.0 |
Mice | 5 | 0.0 |
Refsum Disease/*genetics/metabolism | 2 | 100.0 |
Recombinant Fusion Proteins | 2 | 0.0 |
Mutation/genetics | 2 | 0.0 |
