National Breast Cancer Research Institute, University College Hospital, Galway, Ireland.
UI
MeSH Term
Description
Entries
D009154
Mutation
Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations.
Mutations
D006801
Humans
Members of the species Homo sapiens.
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D016158
Genes, p53
Tumor suppressor genes located on the short arm of human chromosome 17 and coding for the phosphoprotein p53.