Wen Zhai

Terminal 10q26.12 deletion is associated with neonatal asymmetric crying facies syndrome: a case report and literature review

Qinghong Li, Chun-lei Sun, Jinzhen Guo, 2021, Molecular cytogenetics.

The genotype and phenotype of chromosome 18p deletion syndrome

R. Qiang, Wen Zhai, Xiaobin Wang, 2021, Medicine.

Unexpected DMD Gene Mutations Detected by CMA and CNV-seq in amniotic Fluid and Aborted Fetus Samples

Lihui Yang, R. Qiang, Wen Zhai, 2021 .