Latest Copy number variation Stories
Sequenom to apply Cypher's Mantis technology for advanced genome interpretation in NIPT SAN DIEGO, Jan.
SAN DIEGO, Oct.
Rare copy number variations are more common in families that are affected by autism, suggesting that this type of genetic testing could prove to be an important tool in the individualized diagnosis and treatment of the condition.
New study finds substantial proportion of risk for developing autism spectrum disorders resides in genes that are part of specific, interconnected biological pathways New
Researchers at King's College London and Imperial College London have discovered that people with fewer copies of a gene coding for a carb-digesting enzyme may be at higher risk of obesity.
While it was once believed that every cell in a person’s body contains the same DNA code, new research led by experts at the Salk Institute has found an unexpected level of variation among the genomes of different neurons originating from the same person’s brain.
Transparency Market Research published new "Molecular Cytogenetics Market - Global Industry Analysis, Size, Share, Growth, Trends and Forecast, 2013 - 2019" market research report to
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