Search Results - Zongfu Cao

A novel 1.38-kb deletion combined with a single nucleotide variant in KIAA0586 as a cause of Joubert syndrome by Yue Shen, Chao Lu, Tingting Cheng, Zongfu Cao, Cuixia Chen, Xu Ma, Huafang Gao, Minna Luo

Connect to this object online.

Trajectories of peripheral white blood cells count around the menopause: a prospective cohort study by Qiaoyun Dai, Yaya Zhang, Xiujuan Zhao, Xueying Yang, Huayu Sun, Shouling Wu, Shuohua Chen, Jianmei Wang, Zongfu Cao, Xu Ma

Connect to this object online.

Novel mutations in HSF4 cause congenital cataracts in Chinese families by Zongfu Cao, Yihua Zhu, Lijuan Liu, Shuangqing Wu, Bing Liu, Jianfu Zhuang, Yi Tong, Xiaole Chen, Yongqing Xie, Kaimei Nie, Cailing Lu, Xu Ma, Juhua Yang

Connect to this object online.

Detailed pedigree analyses and prenatal diagnosis for a family with mucopolysaccharidosis type II by Chuan Zhang, Shengju Hao, ZhaoYan Meng, Ling Hui, Yan Wang, Feng Xuan, Xue Chen, Xing Wang, Furong Zheng, Lei Zheng, Bingbo Zhou, Xinqi Wu, Qinghua Zhang, Zongfu Cao

Connect to this object online.

Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome by Yue Shen, Hao Wang, Zhimin Liu, Minna Luo, Siyu Ma, Chao Lu, Zongfu Cao, Yufei Yu, Ruikun Cai, Cuixia Chen, Qian Li, Huafang Gao, Yun Peng, Baoping Xu, Xu Ma

Connect to this object online.