Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysis

por MA, DINGYUAN, ZHANG, JINGJING, LUO, CHUNYU, LIN, YING, JI, XIUQING, HU, PING, XU, ZHENGFENG
Publicado 2016

Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing

por Ji, Xiuqing, Liang, Dong, Sun, Ruihong, Liu, Cuiyun, Ma, Dingyuan, Wang, Yan, Hu, Ping, Xu, Zhengfeng
Publicado 2015

11q13.3q13.4 deletion plus 9q21.13q21.33 duplication in an affected girl arising from a familial four‐way balanced chromosomal translocation

por Zhang, Qinxin, Wang, Yan, Zhou, Jing, Zhou, Ran, Liu, An, Meng, Lulu, Ji, Xiuqing, Hu, Ping, Xu, Zhengfeng
Publicado 2023

Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound Anomalies

por Ji, Xiuqing, Pan, Qiong, Wang, Yan, Wu, Yun, Zhou, Jing, Liu, An, Qiao, Fengchang, Ma, Dingyuan, Hu, Ping, Xu, Zhengfeng
Publicado 2018

Optical genome mapping for detection of chromosomal aberrations in prenatal diagnosis

por Zhang, Qinxin, Wang, Yan, Xu, Yiyun, Zhou, Ran, Huang, Mingtao, Qiao, Fengchang, Meng, Lulu, Liu, An, Zhou, Jing, Li, Li, Ji, Xiuqing, Xu, Zhengfeng, Hu, Ping
Publicado 2023