MeSH term
Frequency | Condition_Probility | Acetylation | 2 | 0.0 |
Base Sequence | 10 | 0.0 |
Brain/metabolism | 4 | 0.0 |
DNA Methylation | 5 | 0.0 |
Female | 12 | 0.0 |
Gene Expression | 8 | 0.0 |
Genomic Imprinting | 6 | 3.0 |
Humans | 18 | 0.0 |
Male | 15 | 0.0 |
Phenotype | 6 | 0.0 |
Research Support, Non-U.S. Gov't | 16 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 11 | 0.0 |
*Alleles | 2 | 0.0 |
DNA Primers | 4 | 0.0 |
*Genomic Imprinting | 7 | 2.0 |
Reverse Transcriptase Polymerase Chain Reaction | 2 | 0.0 |
Ribonucleoproteins, Small Nuclear/*genetics | 3 | 17.0 |
Transcription, Genetic | 4 | 0.0 |
Adolescent | 3 | 0.0 |
Adult | 5 | 0.0 |
Child | 2 | 0.0 |
Child, Preschool | 3 | 0.0 |
*Chromosome Aberrations | 2 | 0.0 |
Chromosome Deletion | 2 | 0.0 |
*Chromosomes, Human, Pair 15 | 5 | 2.0 |
Infant | 2 | 0.0 |
Prader-Willi Syndrome/*genetics | 14 | 17.0 |
Alleles | 6 | 0.0 |
Autoantigens/*genetics | 6 | 8.0 |
Polymerase Chain Reaction | 5 | 0.0 |
*Ribonucleoproteins, Small Nuclear | 6 | 11.0 |
Chromosome Banding | 3 | 0.0 |
Chromosomes, Human, Pair 15/*genetics | 3 | 3.0 |
In Situ Hybridization, Fluorescence | 5 | 0.0 |
Molecular Sequence Data | 7 | 0.0 |
Sequence Analysis, DNA | 3 | 0.0 |
*Translocation, Genetic | 4 | 0.0 |
Autoantigens/genetics | 3 | 8.0 |
Cloning, Molecular | 2 | 0.0 |
Conserved Sequence | 3 | 0.0 |
Fathers | 3 | 5.0 |
Open Reading Frames/genetics | 2 | 1.0 |
Transcription Factors/genetics | 2 | 0.0 |
Animals | 6 | 0.0 |
Mice | 5 | 0.0 |
Mice, Inbred C57BL | 2 | 0.0 |
Mice, Inbred Strains | 2 | 0.0 |
Mutagenesis, Site-Directed | 2 | 0.0 |
*Chromosome Deletion | 2 | 0.0 |
Pedigree | 5 | 0.0 |
Chromosomes, Human, Pair 15/genetics | 2 | 2.0 |
Genetic Markers | 2 | 0.0 |
Mothers | 2 | 2.0 |
Blotting, Southern | 2 | 0.0 |
Exons | 2 | 0.0 |
Restriction Mapping | 2 | 0.0 |
DNA | 2 | 0.0 |
Chromosome Mapping | 3 | 0.0 |
Methylation | 3 | 0.0 |
