1. 9th International Congress on Psychopharmacology & 5th International Symposium on Child and Adolescent Psychopharmacology. (31st March 2017) Authors: Baytunca, Muharrem Burak; Kalyoncu, Tugba; Ozel, Ismail; Erermis, Serpil; Kayahan, Bulent; Ongur, Dost; Aykut, Demet Sağlam; Gül, Hasret Karabulut; Elmas, Tuba Şerife; Aydın, Memduha; İlhan, Bilge Çetin; Çokünlü, Yusuf; Eren, İbrahim; Ozdemir, İlker; Gokcen, Onur; Kuru, Erkan; Demir, Erkan; Ünal,... Journal: Psychiatry and clinical psychopharmacology Issue: Volume 27(2017)Supplement 1 Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome. Issue 1 (24th October 2020) Authors: Dyment, David A.; O'Donnell‐Luria, Anne; Agrawal, Pankaj B.; Coban Akdemir, Zeynep; Aleck, Kyrieckos A.; Antaki, Danny; Al Sharhan, Hind; Au, Ping‐Yee B.; Aydin, Hatip; Beggs, Alan H.; Bilguvar, Kaya; Boerwinkle, Eric; Brand, Harrison; Brownstein, Catherine A.; Buyske, Steve; Chodirker, Bernard; ... Journal: American journal of medical genetics Issue: Volume 185:Issue 1(2021) Page Start: 119 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study. (4th July 2017) Authors: Koylu, Mehmet Talay; Kucukevcilioglu, Murat; Erdurman, Fazil Cuneyt; Durukan, Ali Hakan; Sobacı, Gungor; Torun, Deniz; Tunca, Yusuf; Ayyildiz, Onder Journal: Ophthalmic genetics Issue: Volume 38:Number 4(2017) Page Start: 352 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Coexistence of severe developmental delay, epilepsy, and hemangioma in Snijders Blok‐Fisher syndrome suggests the presence of a POU3F3‐related SNIBFIS endophenotype: A case report. Issue 5 (1st March 2021) Authors: Torun, Deniz; Arslan, Mutluay; Yüksel, Zafer Journal: American journal of medical genetics Issue: Volume 185:Issue 5(2021) Page Start: 1554 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Gorlin–chaudhry–moss syndrome revisited: Expanding the phenotype. Issue 7 (17th May 2013) Authors: Rosti, Rasim O.; Karaer, Kadri; Karaman, Birsen; Torun, Deniz; Guran, Sefik; Bahce, Muhterem Journal: American journal of medical genetics Issue: Volume 161:Issue 7(2013:Jul.) Page Start: 1737 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Hypoxia inhibits mineralization ability of human dental pulp cells treated with TEGDMA but increases cell survival in accordance with the culture time. (November 2016) Authors: Öncel Torun, Zeynep; Torun, Deniz; Demirkaya, Kadriye; Yavuz, Süleyman Tolga; Sarper, Meral; Avcu, Ferit Journal: Archives of oral biology Issue: Volume 71(2016) Page Start: 59 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Hypoxia inhibits mineralization ability of human dental pulp cells treated with TEGDMA but increases cell survival in accordance with the culture time. (November 2016) Authors: Öncel Torun, Zeynep; Torun, Deniz; Demirkaya, Kadriye; Yavuz, Süleyman Tolga; Sarper, Meral; Avcu, Ferit Journal: Archives of oral biology Issue: Volume 71(2016) Page Start: 59 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗