MeSH term
Frequency | Condition_Probility | Alleles | 2 | 0.0 |
Chromosomes, Human, Pair 17/genetics | 2 | 1.0 |
Genetic Predisposition to Disease/*genetics | 5 | 1.0 |
Humans | 14 | 0.0 |
Male | 13 | 0.0 |
Amino Acid Sequence | 2 | 0.0 |
Animals | 3 | 0.0 |
Base Sequence | 2 | 0.0 |
Comparative Study | 3 | 0.0 |
Genetic Predisposition to Disease | 6 | 0.0 |
Mice | 2 | 0.0 |
Molecular Sequence Data | 3 | 0.0 |
Mutation, Missense | 2 | 0.0 |
Prostatic Neoplasms/*genetics | 10 | 5.0 |
Research Support, Non-U.S. Gov't | 8 | 0.0 |
Chromosomes, Human, Pair 17/*genetics | 2 | 1.0 |
Genotype | 2 | 0.0 |
Neoplasm Proteins/*genetics | 6 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 4 | 0.0 |
Sequence Analysis, DNA | 3 | 0.0 |
Chromosome Mapping | 2 | 0.0 |
Neoplasm Proteins/genetics | 2 | 0.0 |
Risk Assessment | 3 | 0.0 |
Age of Onset | 2 | 0.0 |
Aged | 4 | 0.0 |
DNA, Neoplasm/chemistry/genetics | 2 | 1.0 |
Family | 2 | 0.0 |
*Genome, Human | 2 | 0.0 |
Linkage (Genetics)/*genetics | 2 | 0.0 |
Middle Aged | 4 | 0.0 |
Polymerase Chain Reaction | 2 | 0.0 |
Case-Control Studies | 2 | 0.0 |
Risk Factors | 3 | 0.0 |