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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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Bibliografske podrobnosti
izdano v:Indian J Med Res
Main Authors: Suresh, Raviraj V., Lingaiah, Kusuma, Veerappa, Avinash M., Ramachandra, Nallur B.
Format: Artigo
Jezik:Inglês
Izdano: Medknow Publications & Media Pvt Ltd 2017
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5460571/
https://ncbi.nlm.nih.gov/pubmed/28574013
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijmr.IJMR_965_14
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