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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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| Publicat a: | Indian J Med Res |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2017
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| Matèries: | |
| Accés en línia: | 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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