1. A novel mutation in the ABCA12 gene in a Turkish case of Harlequin ichthyosis. Issue 3 (July 2015) Authors: Gürkan, Hakan; Fischer, Judith; Ulusal, Selma; Vatansever, Ülfet; Hartmann, Britta; Tozkır, Hilmi; Schlipf, Nina; Acunaş, Betül Ayşe Journal: Clinical dysmorphology Issue: Volume 24:Issue 3(2015:Jul.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel mutation in the ABCA12 gene in a Turkish case of Harlequin ichthyosis. Issue 3 (July 2015) Authors: Gürkan, Hakan; Fischer, Judith; Ulusal, Selma; Vatansever, Ülfet; Hartmann, Britta; Tozkır, Hilmi; Schlipf, Nina; Acunaş, Betül Ayşe Journal: Clinical dysmorphology Issue: Volume 24:Issue 3(2015:Jul.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Identification of a novel homozygous TBC1D24 mutation in a Turkish family with DOORS syndrome. Issue 1 (January 2018) Authors: Atli, Engin; Gurkan, Hakan; Ulusal, Selma; Karal, Yasemin; Atli, Emine I.; Tozkir, Hilmi Journal: Clinical dysmorphology Issue: Volume 27:Issue 1(2018:Jan.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Tetrasomy 18p in a Twin Pregnancy with Diverse Expression in Both Fetuses. (2nd September 2016) Authors: Inan, Cihan; Sayın, N. Cenk; Atlı, Emine; Ulusal, Selma; Erzincan, Selen; Uzun, Isil; Gurkan, Hakan; Varol, Füsun G. Journal: Fetal and pediatric pathology Issue: Volume 35:Number 5(2016) Page Start: 339 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗