1. Novel dominant and recessive variants in human ROBO1 cause distinct neurodevelopmental defects through different mechanisms. Issue 16 (26th March 2022) Authors: Huang, Yan; Ma, Mengqi; Mao, Xiao; Pehlivan, Davut; Kanca, Oguz; Un-Candan, Feride; Shu, Li; Akay, Gulsen; Mitani, Tadahiro; Lu, Shenzhao; Candan, Sukru; Wang, Hua; Xiao, Bo; Lupski, James R; Bellen, Hugo J Journal: Human molecular genetics Issue: Volume 31:Issue 16(2022) Page Start: 2751 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype. (1st May 2015) Authors: Gulec, Elif Yilmaz; Ocak, Zeynep; Candan, Sukru; Ataman, Esra; Yarar, Coskun Journal: International journal of cardiology Issue: Volume 186(2015) Page Start: 13 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Titin truncating mutations: A rare cause of dilated cardiomyopathy in the young. (March 2016) Authors: Fatkin, Diane; Lam, Lien; Herman, Daniel S.; Benson, Craig C.; Felkin, Leanne E.; Barton, Paul J.R.; Walsh, Roddy; Candan, Sukru; Ware, James S.; Roberts, Angharad M.; Chung, Wendy K.; Smoot, Leslie; Bornaun, Helen; Keogh, Anne M.; Macdonald, Peter S.; Hayward, Christopher S.; Seidman, J.G.; Robe... Journal: Progress in pediatric cardiology Issue: Volume 40(2016) Page Start: 41 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗