Runhong Xu

A feasibility study of noninvasive prenatal diagnosis in facioscapulohumeral muscular dystrophy type 1 in a Chinese family

Bo Wang, Yiming Wu, Hui Li, 2022, Frontiers in Genetics.

The prevalence and outcomes of α- and β-thalassemia among pregnant women in Hubei Province, Central China

Miaomiao Chen, Yao Cheng, Guoqiang Sun, 2022, Medicine.

Identification of a novel 10.3 kb deletion causing α0-thalassemia by the third-generation sequencing: pedigree analysis and genetic diagnosis.

Jiaqi Li, Hui Li, Yayun Qin, 2023, Clinical biochemistry.