1. A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia. Issue 2 (17th December 2020) Authors: Lao, Qizong; Mallappa, Ashwini; Rueda Faucz, Fabio; Joyal, Elizabeth; Veeraraghavan, Padmasree; Chen, Wuyan; Merke, Deborah P. Journal: Molecular genetics & genomic medicine Issue: Volume 9:Issue 2(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗