Xiao Dang

The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective Study

C. Liao, Dongzhi Li, F. Fu, 2022, Genes.

Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing

C. Liao, Dongzhi Li, Weiyue Gu, 2022, Frontiers in Genetics.

A heterozygous mutation in NOTCH3 in a Chinese family with CADASIL

Tao Luo, Xiufang Wang, Ping Jing, 2022, Frontiers in Genetics.

Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome

M. Bertini, R. Ferrari, A. Ferlini, 2017, Cardiology.

Identification of an LDLR variant in a Chinese familial hypercholesterolemia and its relation to ROS/NLRP3-Mediated pyroptosis in hepatic cells.

Wenzhuo Cheng, Juyi Li, Chao Liu, 2023, Journal of geriatric cardiology : JGC.