Xiaoyan Huang

Next‐generation sequencing improves molecular epidemiological characterization of thalassemia in Chenzhou Region, P.R. China

Dongzhu Lei, Saijun Liu, Wei Li, 2019, Journal of clinical laboratory analysis.

Noninvasive Prenatal Diagnosis for Duchenne Muscular Dystrophy Based on the Direct Haplotype Phasing

Zhiyu Peng, Min Chen, C. Yin, 2019, bioRxiv.

A Novel Mutation at HBA1: c.349G>T Causing α-Thalassemia in a Chinese Family

Xiaohang Chen, Fengxiang Wei, Z. Yin, 2021, Hemoglobin.

Characterization of a novel HBB:c.194dup variant of the β-globin gene combined with six alpha genes

Shi-ping Chen, Xiaoyan Huang, Jungao Huang, 2022, The Journal of international medical research.

Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln; HBB: c.442T>C)] on the β-Globin Gene

Zhiyu Peng, Jindong Chen, Yan Chen, 2019, Hemoglobin.

Exome sequencing of Saudi Arabian patients with ADPKD

Lusheng Wang, M. Lanktree, B. Keating, 2019, Renal failure.

Carrier rate of thalassemia among 25,910 high school students in Shaoguan area, China.

Zhiyu Peng, Jiufeng Li, Xueqin Guo, 2023, Journal of medical screening.

Haplotype-Based Noninvasive Prenatal Diagnosis for Duchenne Muscular Dystrophy: A pilot study in South China

R. Wu, Zhiyu Peng, Min Chen, 2019, bioRxiv.