Kaili Xie

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

Huanming Yang, Dongzhu Lei, Saijun Liu, 2020, Frontiers in Genetics.

Pregestational screening of hereditary deafness genes carriers in 10,684 normal pregnant women in Zhuzhou, China

Kaili Xie, Mingming Qi, Huimin Lai, 2021, Birth defects research.

Metabolomic analysis-identified 2-hydroxybutyric acid might be a key metabolite of severe preeclampsia

Furong Liang, Kaili Xie, Mingming Qi, 2023, Open life sciences.