MeSH term
Frequency | Condition_Probility | Amino Acid Sequence | 4 | 0.0 |
Base Sequence | 5 | 0.0 |
Chromosomes, Human, Pair 11/genetics | 2 | 0.0 |
Chromosomes, Human, Pair 7/genetics | 2 | 2.0 |
Homeodomain Proteins/*genetics | 8 | 1.0 |
Humans | 23 | 0.0 |
Leukemia, Myeloid/*genetics | 2 | 1.0 |
Molecular Sequence Data | 10 | 0.0 |
Nuclear Pore Complex Proteins/*genetics | 2 | 13.0 |
Research Support, Non-U.S. Gov't | 18 | 0.0 |
Translocation, Genetic/*genetics | 2 | 0.0 |
Alleles | 2 | 0.0 |
Female | 7 | 0.0 |
Male | 9 | 0.0 |
Pedigree | 4 | 0.0 |
Syndrome | 7 | 0.0 |
Urogenital Abnormalities/*genetics | 2 | 13.0 |
Animals | 12 | 0.0 |
Multigene Family | 3 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 8 | 0.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
*Genes, Homeobox | 2 | 0.0 |
Mice | 7 | 0.0 |
Polymerase Chain Reaction | 2 | 0.0 |
Fibroblast Growth Factors/metabolism | 2 | 3.0 |
Mutation | 6 | 0.0 |
*Transcription Factors | 7 | 0.0 |
Adult | 2 | 0.0 |
Cohort Studies | 2 | 0.0 |
*Gene Expression Regulation, Developmental | 2 | 0.0 |
Homozygote | 2 | 0.0 |
In Situ Hybridization | 4 | 0.0 |
Phenotype | 6 | 0.0 |
Time Factors | 3 | 0.0 |
Abnormalities, Multiple/*genetics/radiography | 2 | 33.0 |
DNA Mutational Analysis | 5 | 0.0 |
Foot Deformities, Congenital/*genetics/radiography | 2 | 50.0 |
Hand Deformities, Congenital/*genetics/radiography | 2 | 66.0 |
Mutation/*genetics | 2 | 0.0 |
*Trans-Activators | 2 | 0.0 |
Genes, Homeobox/genetics | 2 | 6.0 |
Cell Division | 2 | 0.0 |
Protein Binding | 2 | 0.0 |
Gene Expression Regulation, Developmental | 3 | 0.0 |
Gene Deletion | 2 | 0.0 |
Infant, Newborn | 2 | 0.0 |
Mice, Mutant Strains | 2 | 0.0 |
Hand Deformities, Congenital/*genetics | 2 | 12.0 |
Hypospadias/*genetics | 2 | 33.0 |
Heterozygote | 2 | 0.0 |
Limb Deformities, Congenital/*genetics | 2 | 10.0 |
Polydactyly/genetics | 2 | 9.0 |
Syndactyly/genetics | 2 | 22.0 |
Homeodomain Proteins/genetics | 2 | 0.0 |
