MeSH term
Frequency | Condition_Probility | Animals | 6 | 0.0 |
Base Sequence | 6 | 0.0 |
Chromosome Mapping | 4 | 0.0 |
DNA Primers | 3 | 0.0 |
*Genomic Imprinting | 7 | 2.0 |
In Situ Hybridization, Fluorescence | 2 | 0.0 |
Mice | 6 | 0.0 |
Mice, Inbred C57BL | 4 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 7 | 0.0 |
Contig Mapping | 2 | 1.0 |
Female | 13 | 0.0 |
Genotype | 5 | 0.0 |
Humans | 26 | 0.0 |
In Situ Hybridization | 2 | 0.0 |
Male | 11 | 0.0 |
Methylation | 3 | 0.0 |
Mice, Transgenic | 2 | 0.0 |
Models, Genetic | 2 | 0.0 |
Mutation | 3 | 0.0 |
Nuclear Proteins/*biosynthesis/*genetics | 2 | 40.0 |
Phenotype | 4 | 0.0 |
Research Support, Non-U.S. Gov't | 23 | 0.0 |
Adult | 7 | 0.0 |
Frameshift Mutation | 2 | 0.0 |
Immunohistochemistry | 4 | 0.0 |
Middle Aged | 2 | 0.0 |
Nuclear Proteins/biosynthesis/*genetics | 2 | 5.0 |
Reverse Transcriptase Polymerase Chain Reaction | 4 | 0.0 |
Amino Acid Sequence | 4 | 0.0 |
Chromosomes, Human, Pair 11/*genetics | 6 | 2.0 |
DNA Mutational Analysis | 4 | 0.0 |
Family Health | 2 | 0.0 |
Insulin-Like Growth Factor II/genetics | 4 | 5.0 |
Nuclear Proteins/*genetics | 6 | 1.0 |
Pedigree | 2 | 0.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
Microsatellite Repeats | 2 | 0.0 |
Nuclear Proteins/analysis/genetics | 2 | 22.0 |
Pregnancy | 2 | 0.0 |
Alleles | 3 | 0.0 |
Beckwith-Wiedemann Syndrome/*genetics | 7 | 15.0 |
Chromosomes, Human, Pair 11 | 2 | 0.0 |
Gene Frequency | 2 | 0.0 |
Genetic Markers | 2 | 0.0 |
Genomic Imprinting | 3 | 1.0 |
*Mutation | 2 | 0.0 |
*Chromosomes, Human, Pair 11 | 3 | 0.0 |
DNA Methylation | 3 | 0.0 |
Gene Expression Regulation, Neoplastic | 3 | 0.0 |
*Gene Silencing | 2 | 1.0 |
Gene Expression Regulation, Developmental | 2 | 0.0 |
Nuclear Proteins/genetics | 5 | 1.0 |
*Organic Cation Transport Proteins | 2 | 7.0 |
Proteins/genetics | 2 | 0.0 |
Tumor Cells, Cultured | 2 | 0.0 |
Comparative Study | 3 | 0.0 |
Insulin-Like Growth Factor II/*genetics | 2 | 1.0 |
Molecular Sequence Data | 6 | 0.0 |
Sequence Analysis, DNA | 2 | 0.0 |
*Variation (Genetics) | 2 | 0.0 |
Genomic Imprinting/genetics | 2 | 11.0 |
*Potassium Channels, Voltage-Gated | 2 | 0.0 |
Adolescent | 3 | 0.0 |
Child | 2 | 0.0 |
Infant | 2 | 0.0 |
Cloning, Molecular | 2 | 0.0 |
Genomic Imprinting/*genetics | 2 | 2.0 |
*Chromosome Mapping | 2 | 0.0 |
Oligonucleotide Array Sequence Analysis | 2 | 0.0 |
Cell Line, Tumor | 2 | 0.0 |
Chromosomes, Human, Pair 11/genetics | 2 | 0.0 |
*DNA Methylation | 2 | 0.0 |
Epigenesis, Genetic | 2 | 7.0 |
