Peng Huang

Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α0-Thalassemia in a Chinese Family

Shang Yi, Sheng He, Chenguang Zheng, 2017, Hemoglobin.

Novel NtA and LG1 Mutations in Agrin in a Single Patient Causes Congenital Myasthenic Syndrome

Aiping Wang, J. Xiong, Liqun Liu, 2020, Frontiers in Neurology.

Characterization of Hb Bart’s Hydrops Fetalis Caused by – –SEA and a Large Novel α0-Thalassemia Deletion

Xiao-Xian Tian, X. Qiu, Sheng He, 2018, Hemoglobin.

The First Case Report of X-Linked Sideroblastic Anemia With Ataxia of Chinese Origin and Literature Review

Qingnan He, J. Xiong, Liqun Liu, 2021, Frontiers in Pediatrics.

Analysis of Clinical and Genetic Characterization of Three Ataxia–Telangiectasia Pedigrees With Novel ATM Gene Mutations

J. Xiong, Liqun Liu, Lu Zhang, 2022, Frontiers in Pediatrics.

First Detection of a Splice Site β-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family

Qiang Zhang, Shang Yi, Sheng He, 2015, Hemoglobin.