MeSH term
Frequency | Condition_Probility | Beckwith-Wiedemann Syndrome/genetics | 4 | 19.0 |
Child | 7 | 0.0 |
Chromosomes, Human, Pair 1 | 2 | 0.0 |
*Genes, Wilms Tumor | 5 | 2.0 |
Genes, p53 | 2 | 0.0 |
Humans | 27 | 0.0 |
Kidney Neoplasms/*genetics | 5 | 2.0 |
Research Support, Non-U.S. Gov't | 12 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 8 | 0.0 |
WAGR Syndrome/genetics | 3 | 60.0 |
Animals | 9 | 0.0 |
Kidney Neoplasms/genetics | 2 | 2.0 |
Mutation | 3 | 0.0 |
Nephroblastoma/*genetics | 8 | 5.0 |
WT1 Proteins | 2 | 0.0 |
Chromosome Mapping | 4 | 0.0 |
*Chromosomes, Human, Pair 11 | 7 | 1.0 |
Mice | 5 | 0.0 |
Genotype | 2 | 0.0 |
Molecular Sequence Data | 4 | 0.0 |
*Promoter Regions (Genetics) | 2 | 0.0 |
*Transcription, Genetic | 2 | 0.0 |
Child, Preschool | 7 | 0.0 |
Female | 7 | 0.0 |
Genetic Markers | 3 | 0.0 |
Male | 9 | 0.0 |
Adult | 4 | 0.0 |
Genes, Wilms Tumor/genetics | 4 | 17.0 |
Base Sequence | 3 | 0.0 |
DNA, Complementary | 2 | 0.0 |
*Gene Deletion | 2 | 0.0 |
Alleles | 2 | 0.0 |
Heterozygote | 5 | 0.0 |
Chromosomes, Human, Pair 11 | 5 | 1.0 |
Genes, Tumor Suppressor | 2 | 0.0 |
Karyotyping | 2 | 0.0 |
Cell Line | 2 | 0.0 |
Translocation, Genetic | 2 | 0.0 |
Binding Sites | 2 | 0.0 |
Mice, Nude | 2 | 0.0 |
Infant | 2 | 0.0 |
Syndrome | 2 | 0.0 |
*Genes, Wilms Tumor/genetics | 2 | 100.0 |
Aged | 2 | 0.0 |
Middle Aged | 2 | 0.0 |
Chromosome Deletion | 2 | 0.0 |