1. Copy number variation plays an important role in clinical epilepsy. Issue 6 (13th June 2014) Authors: Olson, Heather; Shen, Yiping; Avallone, Jennifer; Sheidley, Beth R.; Pinsky, Rebecca; Bergin, Ann M.; Berry, Gerard T.; Duffy, Frank H.; Eksioglu, Yaman; Harris, David J.; Hisama, Fuki M.; Ho, Eugenia; Irons, Mira; Jacobsen, Christina M.; James, Philip; Kothare, Sanjeev; Khwaja, Omar; Lipton, Jon... Journal: Annals of neurology Issue: Volume 75:Issue 6(2014:Jun.) Page Start: 943 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Quantitative evaluation of left ventricular volume and function in middle‐aged healthy chinese people with 3 Tesla MRI. Issue 5 (26th March 2016) Authors: Li, Cai‐Ying; Gao, Bu‐Lang; Guo, Fu‐Qian; Zhang, Xue‐Jing; Fan, Qiong‐Ying; Wu, Bai‐Lin; Xiang, Cheng; Liu, Xiao‐Wei; Pan, Tong Journal: Journal of magnetic resonance imaging Issue: Volume 44:Issue 5(2016) Page Start: 1143 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Rare Deleterious PARD3 Variants in the aPKC‐Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation. Issue 4 (15th February 2017) Authors: Chen, Xiaoli; An, Yu; Gao, Yonghui; Guo, Liu; Rui, Lei; Xie, Hua; Sun, Mei; Lam Hung, Siv; Sheng, Xiaoming; Zou, Jizhen; Bao, Yihua; Guan, Hongyan; Niu, Bo; Li, Zandong; Finnell, Richard H.; Gusella, James F.; Wu, Bai‐Lin; Zhang, Ting Journal: Human mutation Issue: Volume 38:Issue 4(2017) Page Start: 378 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay. Issue 8 (6th September 2013) Authors: An, Yu; Amr, Sami S.; Torres, Alcy; Weissman, Laura; Raffalli, Peter; Cox, Gerald; Sheng, Xiaoming; Lip, Va; Bi, Weimin; Patel, Ankita; Stankiewicz, Pawel; Wu, Bai‐Lin; Shen, Yiping Journal: American journal of medical genetics Issue: Volume 162:Issue 8(2013) Page Start: 832 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗