1. 41. EARLY EXPERIENCES WITH TESTING FOR ANEUPLOIDY IN PREIMPLANTATION GENETIC TESTING FOR INHERITED DISORDERS. (August 2019) Authors: Toft, C.L.F.; Diemer, T.; Ingerslev, H.J.; Pedersen, I.S.; Hnida, C.; Degn, B.; Ernst, A.; Okkels, H. Journal: Reproductive biomedicine online Issue: Volume 39(2019)Supplement 1 Page Start: e52 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel deletion mutation in the ALOX12B gene in a Kurdish family with autosomal recessive congenital ichthyosis. (16th November 2015) Authors: Lolas, I.B.; Sommerlund, M.; Okkels, H.; Ramsing, M.; Petersen, M.B. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 30:Number 11(2016:Nov.) Page Start: e144 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗