1. A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma. (1st January 2015) Authors: Kinsler, V.A.; Drury, S.; Khan, A.; Waelchli, R.; Rukaite, G.; Barnicoat, A.; Lench, N.; Harper, J.I.; O'Shaughnessy, R.F.L. Journal: British journal of dermatology Issue: Volume 172:Number 1(2015:Jan.) Page Start: 262 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma. (9th December 2014) Authors: Kinsler, V.A.; Drury, S.; Khan, A.; Waelchli, R.; Rukaite, G.; Barnicoat, A.; Lench, N.; Harper, J.I.; O'Shaughnessy, R.F.L. Journal: British journal of dermatology Issue: Volume 172:Number 1(2015:Jan.) Page Start: 262 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗