1. A heritable microduplication encompassing TBL1XR1 causes a genomic sister‐disorder for the 3q26.32 microdeletion syndrome. Issue 8 (2nd June 2017) Authors: Riehmer, Vera; Erger, Florian; Herkenrath, Peter; Seland, Saskia; Jackels, Miriam; Wiater, Alfred; Heller, Raoul; Beck, Bodo B.; Netzer, Christian Journal: American journal of medical genetics Issue: Volume 173:Issue 8(2017) Page Start: 2132 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗