A novel NHS mutation causes Nance-Horan Syndrome in a Chinese family

por Tian, Qi, Li, Yunping, Kousar, Rizwana, Guo, Hui, Peng, Fenglan, Zheng, Yu, Yang, Xiaohua, Long, Zhigao, Tian, Runyi, Xia, Kun, Lin, Haiying, Pan, Qian
Publicado 2017

Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model

por Guo, Hui, Wang, Tianyun, Wu, Huidan, Long, Min, Coe, Bradley P., Li, Honghui, Xun, Guanglei, Ou, Jianjun, Chen, Biyuan, Duan, Guiqin, Bai, Ting, Zhao, Ningxia, Shen, Yidong, Li, Yun, Wang, Yazhe, Zhang, Yu, Baker, Carl, Liu, Yanling, Pang, Nan, Huang, Lian, Han, Lin, Jia, Xiangbin, Liu, Cenying, Ni, Hailun, Yang, Xinyi, Xia, Lu, Chen, Jingjing, Shen, Lu, Li, Ying, Zhao, Rongjuan, Zhao, Wenjing, Peng, Jing, Pan, Qian, Long, Zhigao, Su, Wei, Tan, Jieqiong, Du, Xiaogang, Ke, Xiaoyan, Yao, Meiling, Hu, Zhengmao, Zou, Xiaobing, Zhao, Jingping, Bernier, Raphael A., Eichler, Evan E., Xia, Kun
Publicado 2018