MeSH term
Frequency | Condition_Probility | Humans | 33 | 0.0 |
Alanine/genetics | 2 | 1.0 |
Base Sequence | 12 | 0.0 |
DNA/chemistry/genetics | 2 | 0.0 |
DNA Mutational Analysis | 7 | 0.0 |
Family Health | 2 | 0.0 |
Female | 18 | 0.0 |
Genotype | 2 | 0.0 |
Homeodomain Proteins/*genetics | 10 | 2.0 |
Male | 23 | 0.0 |
Molecular Sequence Data | 15 | 0.0 |
Pedigree | 13 | 0.0 |
Peptides/genetics | 2 | 2.0 |
Polydactyly/*genetics/pathology | 2 | 66.0 |
Polymorphism, Genetic | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 27 | 0.0 |
Syndactyly/*genetics/pathology | 3 | 100.0 |
*Transcription Factors | 18 | 1.0 |
Trinucleotide Repeat Expansion/*genetics | 2 | 3.0 |
Alleles | 2 | 0.0 |
Exons/genetics | 2 | 0.0 |
Peptides/*genetics | 3 | 3.0 |
Syndrome | 5 | 0.0 |
Animals | 14 | 0.0 |
*Genes, Homeobox | 5 | 2.0 |
Mice | 9 | 0.0 |
Polymerase Chain Reaction | 4 | 0.0 |
Sequence Alignment | 3 | 0.0 |
Homeodomain Proteins/genetics/*metabolism | 3 | 2.0 |
Mutation | 7 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 7 | 0.0 |
Sequence Deletion | 3 | 0.0 |
Adolescent | 2 | 0.0 |
Amino Acid Sequence | 5 | 0.0 |
Blotting, Southern | 2 | 0.0 |
*Chromosomes, Human, Pair 11 | 2 | 0.0 |
*Chromosomes, Human, Pair 2 | 3 | 1.0 |
Gene Expression Regulation, Leukemic | 2 | 2.0 |
Gene Fusion | 2 | 2.0 |
Homeodomain Proteins/biosynthesis/*genetics | 2 | 9.0 |
RNA, Messenger/genetics | 2 | 0.0 |
Reverse Transcriptase Polymerase Chain Reaction | 2 | 0.0 |
Phenotype | 8 | 0.0 |
Transcription, Genetic | 2 | 0.0 |
Adult | 2 | 0.0 |
Child, Preschool | 3 | 0.0 |
Chromosomes, Human, Pair 2/*genetics | 2 | 1.0 |
In Situ Hybridization, Fluorescence | 3 | 0.0 |
Infant, Newborn | 3 | 0.0 |
Karyotyping | 3 | 0.0 |
Mutation/*genetics | 2 | 0.0 |
Body Patterning | 2 | 3.0 |
Homeodomain Proteins/*genetics/metabolism | 2 | 2.0 |
Homozygote | 3 | 0.0 |
Mice, Mutant Strains | 2 | 0.0 |
Homeodomain Proteins/genetics | 6 | 2.0 |
Polydactyly/*genetics | 4 | 18.0 |
Syndactyly/*genetics | 5 | 38.0 |
Gene Expression Regulation, Developmental | 2 | 0.0 |
Child | 3 | 0.0 |
English Abstract | 2 | 0.0 |
Cell Transformation, Neoplastic/genetics | 2 | 0.0 |
*Nuclear Pore Complex Proteins | 2 | 2.0 |
*Translocation, Genetic | 2 | 0.0 |
Chromosomes, Human, Pair 2 | 3 | 1.0 |
Gene Deletion | 3 | 0.0 |
Genetic Markers | 2 | 0.0 |
Multigene Family | 4 | 0.0 |
Fingers/*abnormalities | 3 | 23.0 |
Linkage (Genetics) | 2 | 0.0 |
Lod Score | 2 | 0.0 |
Toes/*abnormalities | 3 | 27.0 |
Chromosome Mapping | 5 | 0.0 |
Heterozygote | 3 | 0.0 |
*Mutation | 2 | 0.0 |
In Situ Hybridization | 2 | 0.0 |
Transcription Factors/genetics | 3 | 0.0 |
Morphogenesis | 2 | 0.0 |
Haplotypes | 2 | 0.0 |
Hand Deformities, Congenital/*genetics | 2 | 12.0 |
Limb Deformities, Congenital/*genetics | 3 | 15.0 |
Polydactyly/genetics | 2 | 9.0 |
Syndactyly/genetics | 2 | 22.0 |