Copy number variation (CNV) identification, interpretation, and database from Brazilian patients
This study shows the relevance of introducing CNV data from diverse cohorts to improve on the interpretation of clinical impact of genomic variations.
Source: Genetics and Molecular Biology - Category: Genetics & Stem Cells Source Type: research
More News: Biology | Brain | Brazil Health | Databases & Libraries | Genetics | Microdeletion Syndromes | Molecular Biology | Neurology | Study