Sorry, we do not have enough data to show an influence graph for this author.
- Full text PDF available (0)
In recent years copy number variants (CNVs) — gains (duplications) and losses (deletions) — have been recognized as a common group of structural variations in the human genome. CNVs contribute to human phenotype and disease to a larger extent than SNPs. State-of-the-art technology such as array-comparative genomic hybridization (array-CGH) allows screening… (More)