An Examination of the Relationship between Hotspots and Recombination Associated with Chromosome 21 Nondisjunction

Trisomy 21, resulting in Down Syndrome (DS), is the most common autosomal trisomy among live-born infants and is caused mainly by nondisjunction of chromosome 21 within oocytes. Risk factors for nondisjunction depend on the parental origin and type of meiotic error. For errors in the oocyte, increas...

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Hauptverfasser: Oliver, Tiffany Renee, Middlebrooks, Candace D., Tinker, Stuart W., Allen, Emily Graves, Bean, Lora J. H., Begum, Ferdouse, Feingold, Eleanor, Chowdhury, Reshmi, Cheung, Vivian, Sherman, Stephanie L.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Public Library of Science 2014
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Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4057233/
https://ncbi.nlm.nih.gov/pubmed/24926858
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0099560
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