1. Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome. Issue 3 (19th January 2016) Authors: Ali, R.H.; Shah, K.; Nasir, A.; Steyaert, W.; Coucke, P.J.; Ahmad, W. Journal: Clinical genetics Issue: Volume 90:Issue 3(2016) Page Start: 263 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗