Manman Li

Prenatally diagnosed 16p11.2 copy number variations by SNP Array: A retrospective case series.

Hong Yan, Hui Li, Yanduo Gao, 2022, Clinica chimica acta; international journal of clinical chemistry.

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.

MiR-301a-3p in the pathogenesis of bacterial meningitis by targeting Cx43

T. Jia, K. Du, Jun Wang, 2019, Neuroreport.