Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma

Genetics in Medicine, Published online: 20 April 2021; doi:10.1038/s41436-021-01175-0

Source: Genetics in Medicine - April 20, 2021 Category: Genetics & Stem Cells Authors: D. Gareth Evans Ludwine M. Messiaen William D. Foulkes Rachel E. A. Irving Alexandra J. Murray Cristina Perez-Becerril Barbara Rivera Donna M. McDonald-McGinn David A. Stevenson Miriam J. Smith Source Type: research