1. DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics. (21st January 2014) Authors: Vona, B.; Hofrichter, M.A.H.; Neuner, C.; Schröder, J.; Gehrig, A.; Hennermann, J.B.; Kraus, F.; Shehata‐Dieler, W.; Klopocki, E.; Nanda, I.; Haaf, T. Journal: Clinical genetics Issue: Volume 87:Number 1(2015:Jan.) Page Start: 49 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗