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Publikováno v:
Frontiers in Genetics, Vol 5 (2014)
Copy number variations (CNVs) constitute a major source of genetic variations in human populations and have been reported to be associated with complex diseases. Methods have been developed for detecting CNVs and testing CNV associations in genome-wi
Externí odkaz:
https://doaj.org/article/d7128c50152b4e4eb99876c34faff6b4