MeSH term
Frequency | Condition_Probility | Adolescent | 4 | 0.0 |
Adult | 8 | 0.0 |
Child | 5 | 0.0 |
Child, Preschool | 2 | 0.0 |
DNA-Binding Proteins/*genetics | 9 | 0.0 |
Female | 13 | 0.0 |
Humans | 27 | 0.0 |
Infant | 3 | 0.0 |
Linkage (Genetics)/*genetics | 2 | 0.0 |
Male | 14 | 0.0 |
Phenotype | 7 | 0.0 |
Research Support, Non-U.S. Gov't | 20 | 0.0 |
Syndrome | 4 | 0.0 |
Transcription Factors/*genetics | 10 | 0.0 |
Adipocytes/*metabolism | 2 | 4.0 |
Animals | 11 | 0.0 |
Mice | 10 | 0.0 |
Aged | 2 | 0.0 |
Aged, 80 and over | 2 | 0.0 |
DNA Mutational Analysis | 4 | 0.0 |
Eyelashes/*abnormalities | 2 | 100.0 |
Family Health | 2 | 0.0 |
Middle Aged | 6 | 0.0 |
Mutation | 2 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 12 | 0.0 |
Blotting, Northern | 2 | 0.0 |
Insulin Resistance/*genetics | 2 | 2.0 |
Mice, Inbred C57BL | 2 | 0.0 |
Mice, Transgenic | 4 | 0.0 |
Cells, Cultured | 3 | 0.0 |
Comparative Study | 2 | 0.0 |
DNA-Binding Proteins/*genetics/metabolism | 2 | 0.0 |
Disease Models, Animal | 3 | 0.0 |
In Situ Hybridization | 3 | 0.0 |
Mice, Mutant Strains | 4 | 0.0 |
Transcription Factors/*genetics/metabolism | 2 | 0.0 |
Base Sequence | 6 | 0.0 |
Chromosomes, Human, Pair 16/genetics | 2 | 2.0 |
Cleft Palate/genetics | 3 | 12.0 |
Lymphedema/*genetics | 2 | 66.0 |
Molecular Sequence Data | 6 | 0.0 |
Mutation/*genetics | 2 | 0.0 |
Polymerase Chain Reaction | 2 | 0.0 |
Genotype | 3 | 0.0 |
Germany | 2 | 0.0 |
Pedigree | 5 | 0.0 |
DNA-Binding Proteins/*genetics/physiology | 3 | 3.0 |
Heterozygote | 4 | 0.0 |
Intraocular Pressure/genetics | 2 | 50.0 |
Transcription Factors/*genetics/physiology | 3 | 3.0 |
Gene Expression Regulation, Developmental | 2 | 0.0 |
Homozygote | 2 | 0.0 |
Mice, Knockout | 2 | 0.0 |
Models, Biological | 2 | 0.0 |
DNA Primers | 2 | 0.0 |
Glucose Tolerance Test | 2 | 0.0 |
Reverse Transcriptase Polymerase Chain Reaction | 2 | 0.0 |
Genes, Dominant | 2 | 0.0 |
Lymphatic Abnormalities/genetics/pathology | 2 | 100.0 |
Adipocytes/metabolism | 2 | 4.0 |
Muscle, Skeletal/metabolism | 2 | 1.0 |
Signal Transduction/*physiology | 2 | 0.0 |
Amino Acid Sequence | 2 | 0.0 |
Models, Molecular | 2 | 0.0 |
Genetic Markers | 2 | 0.0 |
*Mutation, Missense | 2 | 0.0 |