MeSH term
Frequency | Condition_Probility | Amino Acid Sequence | 4 | 0.0 |
Animals | 8 | 0.0 |
Drosophila Proteins/*genetics | 3 | 16.0 |
Epilepsy/*genetics | 3 | 9.0 |
Female | 7 | 0.0 |
Haplotypes | 2 | 0.0 |
Humans | 23 | 0.0 |
Male | 12 | 0.0 |
Mental Retardation/*genetics | 3 | 1.0 |
Mice | 7 | 0.0 |
Models, Genetic | 2 | 0.0 |
Molecular Sequence Data | 6 | 0.0 |
*Mutation | 3 | 0.0 |
Mutation, Missense | 3 | 0.0 |
Pedigree | 6 | 0.0 |
Research Support, Non-U.S. Gov't | 14 | 0.0 |
Sequence Homology, Amino Acid | 3 | 0.0 |
*X Chromosome | 2 | 0.0 |
Child | 4 | 0.0 |
Mutation | 4 | 0.0 |
Comparative Study | 3 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 7 | 0.0 |
X Chromosome/*genetics | 4 | 1.0 |
Adult | 3 | 0.0 |
Aged | 3 | 0.0 |
Middle Aged | 2 | 0.0 |
Cerebral Cortex/*abnormalities | 2 | 25.0 |
Homeodomain Proteins/genetics | 2 | 0.0 |
Infant, Newborn | 6 | 0.0 |
Phenotype | 5 | 0.0 |
Transcription Factors/genetics | 2 | 0.0 |
Abnormalities, Multiple/*genetics | 2 | 0.0 |
Genes, Homeobox/*genetics | 3 | 4.0 |
Homeodomain Proteins/*genetics | 5 | 1.0 |
Transcription Factors/*genetics | 5 | 0.0 |
Child, Preschool | 2 | 0.0 |
DNA Mutational Analysis | 2 | 0.0 |
Genotype | 2 | 0.0 |
Infant | 5 | 0.0 |
Spasms, Infantile/genetics | 3 | 75.0 |
Cells, Cultured | 3 | 0.0 |
Embryo | 2 | 0.0 |
Magnetic Resonance Imaging | 2 | 0.0 |
Mutation/*genetics | 2 | 0.0 |
Autistic Disorder/genetics | 2 | 14.0 |
Epilepsy/genetics | 2 | 11.0 |
Cell Movement | 2 | 0.0 |
Mental Retardation, X-Linked/*genetics | 2 | 10.0 |
Transfection | 2 | 0.0 |
Linkage (Genetics)/*genetics | 2 | 0.0 |
Syndrome | 2 | 0.0 |
Base Sequence | 3 | 0.0 |
Genes, Homeobox | 3 | 3.0 |
Spasms, Infantile/*genetics | 2 | 33.0 |
*Genes, Homeobox | 2 | 0.0 |
