1. Homozygous XYLT2 variants as a cause of spondyloocular syndrome. Issue 4 (20th February 2018) Authors: Umair, M.; Eckstein, G.; Rudolph, G.; Strom, T.; Graf, E.; Hendig, D.; Hoover, J.; Alanay, J.; Meitinger, T.; Schmidt, H.; Ahmad, W. Journal: Clinical genetics Issue: Volume 93:Issue 4(2018) Page Start: 913 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗