MeSH term
Frequency | Condition_Probility | Chromosome Mapping | 8 | 0.0 |
Humans | 23 | 0.0 |
Mandibulofacial Dysostosis/genetics | 2 | 66.0 |
Polymorphism, Single-Stranded Conformational | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 16 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 13 | 0.0 |
Adult | 2 | 0.0 |
Child | 2 | 0.0 |
Female | 9 | 0.0 |
Male | 9 | 0.0 |
Mandibulofacial Dysostosis/*genetics | 12 | 85.0 |
Nuclear Proteins/*genetics | 5 | 0.0 |
Pedigree | 5 | 0.0 |
Phenotype | 2 | 0.0 |
Phosphoproteins/*genetics | 5 | 2.0 |
Amino Acid Sequence | 7 | 0.0 |
Animals | 10 | 0.0 |
Cloning, Molecular | 4 | 0.0 |
Exons/genetics | 2 | 0.0 |
Gene Library | 3 | 0.0 |
In Situ Hybridization, Fluorescence | 3 | 0.0 |
Introns/genetics | 2 | 0.0 |
Molecular Sequence Data | 13 | 0.0 |
Exons | 3 | 0.0 |
Mice | 7 | 0.0 |
Mice, Inbred C57BL | 3 | 0.0 |
*Mutation | 3 | 0.0 |
Hela Cells | 2 | 0.0 |
Base Sequence | 11 | 0.0 |
DNA Primers | 4 | 0.0 |
Phosphorylation | 2 | 0.0 |
Recombinant Fusion Proteins/genetics | 2 | 1.0 |
Green Fluorescent Proteins | 2 | 0.0 |
Sequence Homology, Amino Acid | 5 | 0.0 |
Polymerase Chain Reaction | 5 | 0.0 |
Embryo/metabolism | 2 | 1.0 |
Sequence Analysis, DNA | 3 | 0.0 |
DNA, Complementary | 2 | 0.0 |
Syndrome | 2 | 0.0 |
Chromosomes, Human, Pair 5 | 2 | 1.0 |
Genetic Markers | 2 | 0.0 |
Polymorphism, Genetic | 2 | 0.0 |
Exons/*genetics | 2 | 0.0 |
Mutation | 2 | 0.0 |
Restriction Mapping | 2 | 0.0 |
*Chromosomes, Human, Pair 5 | 5 | 2.0 |
Linkage (Genetics) | 3 | 0.0 |
Cosmids | 2 | 0.0 |
