1. Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome. (1st June 2021) Authors: Vornweg, J.; Gläser, S.; Ahmad‐Anwar, M.; Zimmer, A.D.; Kuhn, M.; Hörer, S.; Korenke, G.C.; Grothaus, J.; Ott, H.; Fischer, J. Journal: British journal of dermatology Issue: Volume 184:Number 6(2021) Page Start: 1190 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome. (3rd March 2021) Authors: Vornweg, J.; Gläser, S.; Ahmad‐Anwar, M.; Zimmer, A.D.; Kuhn, M.; Hörer, S.; Korenke, G.C.; Grothaus, J.; Ott, H.; Fischer, J. Journal: British journal of dermatology Issue: Volume 184:Number 6(2021) Page Start: 1190 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Paediatric lichen sclerosus: a systematic review of 4516 cases. (11th September 2019) Authors: Balakirski, G.; Grothaus, J.; Altengarten, J.; Ott, H. Journal: British journal of dermatology Issue: Volume 182:Number 1(2020) Page Start: 231 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Paediatric lichen sclerosus: a systematic review of 4516 cases. (1st January 2020) Authors: Balakirski, G.; Grothaus, J.; Altengarten, J.; Ott, H. Journal: British journal of dermatology Issue: Volume 182:Number 1(2020) Page Start: 231 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗