Huazhong Ma

Case Report: A Novel PAX3 Mutation Associated With Waardenburg Syndrome Type 1

Haoyu Li, Zongming Zhuang, Qiuming Hu, 2021, Frontiers in Genetics.

Novel genotypes and phenotypes among Chinese patients with Floating-Harbor syndrome

Yiping Shen, Jian Wang, Haiming Yuan, 2019, Orphanet Journal of Rare Diseases.

GW29-e0750 The CACNA1D exon mutations are possible novel risk locus for preeclampsia

Hui Chen, Huazhong Ma, Huan Wang, 2018, Journal of the American College of Cardiology.