1. Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A. Issue 7 (6th May 2019) Authors: Golas, Monika M.; Auber, Bernd; Ripperger, Tim; Pabst, Brigitte; Schmidt, Gunnar; Morlot, Michel; Diebold, Uta; Steinemann, Doris; Schlegelberger, Brigitte; Morlot, Susanne Journal: American journal of medical genetics Issue: Volume 179:Issue 7(2019) Page Start: 1383 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗