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Chromosomal drive and the evolution of meiotic nondisjunction and trisomy in humans

Trisomy is a genetic abnormality of considerable medical importance. The most familiar example is trisomy 21, which causes Down Syndrome [Cummings, M. R. (1988) Human Heredity: Principles and Issues (West Publishing Company, New York)]. In a classic paper, Axelrod and Hamilton [Axelrod, R. & Ham...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Day, Troy, Taylor, Peter D.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The National Academy of Sciences 1998
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC19347/
https://ncbi.nlm.nih.gov/pubmed/9482890
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