Novel phenotypes of NF1 patients from unrelated Chinese families with tibial pseudarthrosis and anemia

por Banerjee, Santasree, Lei, Dongzhu, Liang, Shengran, Yang, Li, Liu, Saijun, Wei, Zhu, Tang, Jian Ping
Publicado 2016

46,XX Testicular Disorders of Sex Development With DMD Gene Mutation: First Case Report Identified Prenatally by Integrated Analyses in China

por Deng, Jianlian, Zhang, Haoqing, Li, Caiyun, Huang, Hui, Liu, Saijun, Yang, Huanming, Xie, Kaili, Wang, Qiong, Lei, Dongzhu, Wu, Jing
Publicado 2020

The effect of hemolysis on quality control metrics for noninvasive prenatal testing

por Guo, Yaya, Yu, Dandan, Zhou, Kaisu, Wang, Jie, Lei, Dongzhu, Xu, Zhenpeng, Tang, Weijiang, Wu, Miaofeng, Fang, Xingxing, Shen, Jiankun, Peng, Zhiyu, Xiang, Jiale
Publicado 2022

Clinical and genomic evaluation of a Chinese patient with a novel deletion associated with Phelan–McDermid syndrome

por Lei, Dongzhu, Li, Shaoyuan, Banerjee, Santasree, Zhang, Haoqing, Li, Caiyun, Hou, Shuai, Chen, Danjing, Yan, Haiying, Li, Hanmei, peng, Huan Huan, Liu, Saijun, Zhang, Xinxin, Peng, Zhiyu, Wang, Jian, Yang, Huanming, Huang, Hui, Wu, Jing
Publicado 2016

Next‐generation sequencing improves molecular epidemiological characterization of thalassemia in Chenzhou Region, P.R. China

por Zhang, Haoqing, Li, Caiyun, Li, Jianbiao, Hou, Shuai, Chen, Danjing, Yan, Haiying, Chen, Shiping, Liu, Saijun, Yin, Zhenzhen, Yang, Xiaoqin, Tan, Jufang, Huang, Xiaoyan, Zhang, Liming, Fang, Junbin, Zhang, Caifen, Li, Wei, Guo, Jian, Lei, Dongzhu
Publicado 2019