1. Screening for single nucleotide variants, small indels and exon deletions with a next‐generation sequencing based gene panel approach for Usher syndrome. Issue 5 (15th June 2014) Authors: Krawitz, Peter M.; Schiska, Daniela; Krüger, Ulrike; Appelt, Sandra; Heinrich, Verena; Parkhomchuk, Dmitri; Timmermann, Bernd; Millan, Jose M.; Robinson, Peter N.; Mundlos, Stefan; Hecht, Jochen; Gross, Manfred Journal: Molecular genetics & genomic medicine Issue: Volume 2:Issue 5(2014:Sep.) Page Start: 393 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗