A novel mutation in a common pathogenic gene (SETD5) associated with intellectual disability: A case report

af Fang, Yu-Lian, Zhang, Rui-Ping, Wang, Yi-Zheng, Cao, Li-Rong, Zhang, Yu-Qin, Cai, Chun-Quan
Udgivet i Exp Ther Med (2019)

Association of neural tube defects with maternal alterations and genetic polymorphisms in one-carbon metabolic pathway

af Cai, Chun-Quan, Fang, Yu-Lian, Shu, Jian-Bo, Zhao, Lin-Sheng, Zhang, Rui-Ping, Cao, Li-Rong, Wang, Yi-Zheng, Zhi, Xiu-Fang, Cui, Hua-Lei, Shi, Ou-Yan, Liu, Wei
Udgivet i Ital J Pediatr (2019)