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Genetic Structures of Copy Number Variants Revealed by Genotyping Single Sperm

BACKGROUND: Copy number variants (CNVs) occupy a significant portion of the human genome and may have important roles in meiotic recombination, human genome evolution and gene expression. Many genetic diseases may be underlain by CNVs. However, because of the presence of their multiple copies, varia...

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Bibliografiske detaljer
Main Authors: Luo, Minjie, Cui, Xiangfeng, Fredman, David, Brookes, Anthony J., Azaro, Marco A., Greenawalt, Danielle M., Hu, Guohong, Wang, Hui-Yun, Tereshchenko, Irina V., Lin, Yong, Shentu, Yue, Gao, Richeng, Shen, Li, Li, Honghua
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2009
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2668179/
https://ncbi.nlm.nih.gov/pubmed/19384415
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0005236
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