Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing

por Zhao, Pingsen, Lin, Lifang, Lan, Liubing
Publicado 2018

Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing

por Lan, Liubing, She, Lingna, Zhang, Bosen, He, Yanhong, Zheng, Zhiyuan
Publicado 2021

Analysis of copy number variation by sequencing in fetuses with nuchal translucency thickening

por Lan, Liubing, Wu, Heming, She, Lingna, Zhang, Bosen, He, Yanhong, Luo, Dandan, Wang, Huaxian, Zheng, Zhiyuan
Publicado 2020

Invasive molecular prenatal diagnosis of alpha and beta thalassemia among Hakka pregnant women

por Wu, Heming, Wang, Huaxian, Lan, Liubing, Zeng, Mei, Guo, Wei, Zheng, Zhiyuan, Zhu, Huichao, Wu, Jie, Zhao, Pingsen
Publicado 2018