Nondisjunction, Genetic

MeSH 搜索器

Nondisjunction, Genetic

The failure of homologous CHROMOSOMES or CHROMATIDS to segregate during MITOSIS or MEIOSIS with the result that one daughter cell has both of a pair of parental chromosomes or chromatids and the other has none.

推出的年份: 1982

副标题

drug effects

ethics

genetics

immunology

physiology

radiation effects

树号: C23.550.210.645, G05.113.220.625.620, G05.558.620

MeSH 单一 ID: D009630

进入的组:

Genetic Nondisjunctions
Nondisjunctions, Genetic
Genetic Nondisjunction
Genetic Non-Disjunction
Genetic Non Disjunction
Genetic Non-Disjunctions
Non-Disjunctions, Genetic
Non-Disjunction, Genetic
Non Disjunction, Genetic

早前的内容:

Cell Division (1966-1967)
Chromosome Aberrations (1968-1981)
Chromosomes (1966-1967)
Meiosis (1968-1981)

All MeSH Categories
- Diseases Category
  - Pathological Conditions, Signs and Symptoms [C23]
    - Pathologic Processes [C23.550]
      - Chromosome Aberrations [C23.550.210]

All MeSH Categories
- Phenomena and Processes
  - Genetic Phenomena [G05]
    - Cell Division [G05.113]
      - Cell Nucleus Division [G05.113.220]
        
        Chromosome Segregation [G05.113.220.625]
        
        Nondisjunction, Genetic [G05.113.220.625.620]

All MeSH Categories
- Phenomena and Processes
  - Genetic Phenomena [G05]
    - Mutagenesis [G05.558]

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MeSH 搜索器

Nondisjunction, Genetic

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