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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Detalles Bibliográficos
Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668179/
https://www.ncbi.nlm.nih.gov/pubmed/19384415
http://dx.doi.org/10.1371/journal.pone.0005236

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668179/
https://www.ncbi.nlm.nih.gov/pubmed/19384415
http://dx.doi.org/10.1371/journal.pone.0005236

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