A novel splicing variation in L1CAM is responsible for recurrent fetal hydrocephalus

por He, Tiantian, Yao, Qiang, Xu, Bocheng, Yang, Mei, Jiang, Jieni, Xiang, Qingqing, Xiao, Like, Liu, Shanling, Wang, He, Zhang, Xuemei
Publicado 2023

Clinical experience of noninvasive prenatal testing for rare chromosome abnormalities in singleton pregnancies

por Hu, Ting, Wang, Jiamin, Zhu, Qian, Zhang, Zhu, Hu, Rui, Xiao, Like, Yang, Yunyuan, Liao, Na, Liu, Sha, Wang, He, Niu, Xiaoyu, Liu, Shanling
Publicado 2022

A chromosomal microarray analysis-based laboratory algorithm for the detection of genetic etiology of early pregnancy loss

por Liao, Na, Zhang, Zhu, Liu, Xijing, Wang, Jiamin, Hu, Rui, Xiao, Like, Yang, Yunyuan, Lai, Yi, Zhu, Hongmei, Li, Lingping, Liu, Shanling, Wang, He, Hu, Ting
Publicado 2023