1. Loeys–Dietz syndrome caused by 1q41 deletion including TGFB2 is associated with a neurodevelopmental phenotype. Issue 7 (15th April 2022) Authors: Fry, Deanna; Groepper, Daniel; MacCarrick, Gretchen; Demo, Erin M.; Thomas, Matthew J.; Wilkes, Margaret J.; Lyons, Michael J.; Tucker, Megan E.; Steding, Catherine; Fleischer, Julie Journal: American journal of medical genetics Issue: Volume 188:Issue 7(2022) Page Start: 2237 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗