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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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Detalles Bibliográficos
Autores principales:	Suresh, Raviraj V., Lingaiah, Kusuma, Veerappa, Avinash M., Ramachandra, Nallur B.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2017
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460571/ https://www.ncbi.nlm.nih.gov/pubmed/28574013 http://dx.doi.org/10.4103/ijmr.IJMR_965_14

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