MeSH term
Frequency | Condition_Probility | Homeodomain Proteins/genetics | 3 | 1.0 |
Humans | 11 | 0.0 |
Research Support, Non-U.S. Gov't | 7 | 0.0 |
Chromosomes, Human, Pair 2/genetics | 2 | 1.0 |
Chromosomes, Human, Pair 3/genetics | 2 | 1.0 |
Chromosomes, Human, Pair 7/genetics | 2 | 2.0 |
Female | 6 | 0.0 |
Foot Deformities, Congenital/*genetics | 7 | 53.0 |
Karyotyping | 2 | 0.0 |
Male | 7 | 0.0 |
Pedigree | 5 | 0.0 |
Chromosome Mapping | 5 | 0.0 |
Hand Deformities, Congenital/*genetics | 6 | 37.0 |
In Situ Hybridization, Fluorescence | 3 | 0.0 |
*Chromosomes, Human, Pair 10 | 3 | 1.0 |
Linkage (Genetics) | 2 | 0.0 |
Abnormalities, Multiple/*genetics/pathology | 2 | 2.0 |
*Chromosomes, Human, Pair 7 | 2 | 0.0 |
Infant, Newborn | 3 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 3 | 0.0 |
Abnormalities, Multiple/*genetics | 2 | 0.0 |
