MeSH term
Frequency | Condition_Probility | Animals | 10 | 0.0 |
Base Sequence | 6 | 0.0 |
Humans | 16 | 0.0 |
Molecular Sequence Data | 9 | 0.0 |
Promoter Regions (Genetics) | 2 | 0.0 |
Proteins/*genetics | 10 | 0.0 |
Research Support, Non-U.S. Gov't | 14 | 0.0 |
Cell Cycle Proteins/*genetics | 3 | 1.0 |
Cell Line | 2 | 0.0 |
Chromosomes, Human, Pair 22/genetics | 2 | 2.0 |
Conserved Sequence | 2 | 0.0 |
DiGeorge Syndrome/*genetics | 2 | 4.0 |
Gene Expression Regulation, Developmental | 6 | 0.0 |
Mice | 7 | 0.0 |
Phenotype | 4 | 0.0 |
RNA, Messenger/genetics/metabolism | 3 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 7 | 0.0 |
Sequence Deletion | 2 | 0.0 |
Transcription, Genetic | 3 | 0.0 |
Amino Acid Sequence | 5 | 0.0 |
Blotting, Northern | 2 | 0.0 |
Chromosome Banding | 2 | 0.0 |
Chromosome Mapping | 5 | 0.0 |
Cloning, Molecular | 5 | 0.0 |
DNA, Complementary/genetics | 2 | 0.0 |
Female | 2 | 0.0 |
Gene Expression | 3 | 0.0 |
In Situ Hybridization, Fluorescence | 3 | 0.0 |
Nuclear Proteins/*genetics/metabolism | 2 | 1.0 |
Sequence Alignment | 2 | 0.0 |
Sequence Homology, Amino Acid | 3 | 0.0 |
Syndrome | 4 | 0.0 |
Tissue Distribution | 2 | 0.0 |
DNA/genetics | 2 | 0.0 |
Green Fluorescent Proteins | 2 | 0.0 |
Luminescent Proteins/genetics/metabolism | 2 | 1.0 |
Male | 2 | 0.0 |
Polymorphism, Genetic | 2 | 0.0 |
Recombinant Fusion Proteins/genetics/metabolism | 2 | 0.0 |
Heart Defects, Congenital/*genetics | 3 | 7.0 |
*Chromosome Deletion | 2 | 0.0 |
Chromosomes, Human, Pair 22/*genetics | 2 | 2.0 |
Comparative Study | 2 | 0.0 |
Craniofacial Abnormalities/*genetics | 3 | 9.0 |
*Chromosomes, Human, Pair 22 | 3 | 1.0 |
*Gene Deletion | 2 | 0.0 |
DNA, Complementary | 2 | 0.0 |
