1. A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis. Issue 4 (1st April 2016) Authors: Sun, Yu-Min; Wang, Jun; Qiu, Xing-Biao; Yuan, Fang; Li, Ruo-Gu; Xu, Ying-Jia; Qu, Xin-Kai; Shi, Hong-Yu; Hou, Xu-Min; Huang, Ri-Tai; Xue, Song; Yang, Yi-Qing Journal: G3 Issue: Volume 6:Issue 4(2016) Page Start: 987 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations. (3rd April 2017) Authors: Li, Yan-Jie; Yang, Yi-Qing Journal: Expert review of molecular diagnostics Issue: Volume 17:Number 4(2017) Page Start: 393 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. On the Maturation of Megakaryocytes: A Review with Original Observations on Human In Vivo Cells Emphasizing Morphology and Ultrastructure. (April 2015) Authors: Ru, Yong-Xin; Zhao, Shi-Xuan; Dong, Shu-Xu; Yang, Yi-Qing; Eyden, Brian Journal: Ultrastructural pathology Issue: Volume 39:Number 2(2015:Apr.) Page Start: 79 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. SMAD1 Loss-of-Function Variant Responsible for Congenital Heart Disease. (3rd March 2022) Authors: Wang, Zhi; Qiao, Xiao-Hui; Xu, Ying-Jia; Liu, Xing-Yuan; Huang, Ri-Tai; Xue, Song; Qiu, Hai-Yan; Yang, Yi-Qing Other Names: Aga Syed Sameer Academic Editor. Journal: BioMed research international Issue: Volume 2022(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗