Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approach

Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approach

Background & objectives: Aneuploids are the most common chromosomal abnormality in liveborns and are usually the result of non-disjunction (NDJ) in meiosis. Copy number variations (CNVs) are large structural variations affecting the human genome. CNVs influence critical genes involved in causing...

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Bibliographic Details
Main Authors: Raviraj V Suresh, Kusuma Lingaiah, Avinash M Veerappa, Nallur B Ramachandra
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Indian Journal of Medical Research
Subjects:
Aneuploidy - copy number variations - meiotic recombination - non-disjunction
Online Access:http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2017;volume=145;issue=1;spage=39;epage=50;aulast=Suresh

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http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2017;volume=145;issue=1;spage=39;epage=50;aulast=Suresh

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