Identification of copy number variants associated with renal agenesis using array-based comparative genomic hybridization
Copy Number Variants (CNVs) are defined as DNA segments of 1kb or more in length and present in a variable number of copies in the human genome. It has been recently shown that many human genetic diseases including organ malformations are caused by CNVs in a patient's genome. However, the genet...
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| Language: | English |
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University of Iowa
2010
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| Online Access: | https://ir.uiowa.edu/etd/655 https://ir.uiowa.edu/cgi/viewcontent.cgi?article=1840&context=etd |