Mei-jiao Cai

A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy

Yanru Huang, Ping Li, Xiaomin Ma, 2021, Frontiers in Genetics.

Pedigree analysis of two brothers with severe oligozoospermia caused by maternal inv(X) (p22.3, q22) chromosome abnormality

Y. Sha, Yun-sheng Ge, Xiaolu Chen, 2020, Andrologia.

A novel electrochemical immunoassay for carcinoembryonic antigen based on glucose oxidase-encapsulated nanogold hollow spheres with a pH meter readout.

Jian Zhang, Yu Jiang, Zhiying Su, 2018, The Analyst.

Retrospective study revealed integration of CNV-seq and karyotype analysis is an effective strategy for prenatal diagnosis of chromosomal abnormalities

Jian Zhang, Mei-jiao Cai, Jiayan Chen, 2024, Frontiers in genetics.