Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida

Genetics in Medicine, Published online: 08 March 2021; doi:10.1038/s41436-021-01126-9Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida

Source: Genetics in Medicine - March 8, 2021 Category: Genetics & Stem Cells Authors: Paul Wolujewicz Vanessa Aguiar-Pulido Alice AbdelAleem Vidya Nair Gaurav Thareja Karsten Suhre Gary M. Shaw Richard H. Finnell Olivier Elemento M. Elizabeth Ross Source Type: research