Visningssätt för begreppens/termernas förhållanden:
Det sätt begreppsrelationer visas:
Det sätt begreppsrelationer visas:
Mutation
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Bredare villkor: | |
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Anmärkning: | 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.
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Annotation: | drug-induced mutation = MUTATION (IM) + specific drug with pertinent qualif (IM); radiation-induced mutation = MUTATION (IM) + RADIATION EFFECTS or specific rad term (IM); /drug eff & /rad eff permitted only for eff of drugs or eff of rad on an already mutated organism or after mutation but read text carefully
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historyNote*: | 64
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publicMeSHNote*: | 64
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1964-01-01X |
dateRevised*: | 2003-07-09X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | NLMX |
Relaterad term: | |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Mutaatio (fi) XMutaatiot (fi, ersatt) |
Dela: |
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