"Nondisjunction, Genetic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
- Nondisjunction, Genetic
- Genetic Nondisjunctions
- Nondisjunctions, Genetic
- Genetic Nondisjunction
- Genetic Non-Disjunction
- Genetic Non Disjunction
- Genetic Non-Disjunctions
- Non-Disjunctions, Genetic
- Non-Disjunction, Genetic
- Non Disjunction, Genetic
Below are MeSH descriptors whose meaning is more general than "Nondisjunction, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Nondisjunction, Genetic".
This graph shows the total number of publications written about "Nondisjunction, Genetic" by people in this website by year, and whether "Nondisjunction, Genetic" was a major or minor topic of these publications.
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Below are the most recent publications written about "Nondisjunction, Genetic" by people in Profiles.
Sheridan MB, Kato T, Haldeman-Englert C, Jalali GR, Milunsky JM, Zou Y, Klaes R, Gimelli G, Gimelli S, Gemmill RM, Drabkin HA, Hacker AM, Brown J, Tomkins D, Shaikh TH, Kurahashi H, Zackai EH, Emanuel BS. A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21). Am J Hum Genet. 2010 Aug 13; 87(2):209-18.