T. Zeng

Clinical and immunological characteristics of five patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China–expanding the atypical phenotypes

Xiaodong Zhao, Lina Zhou, Xuemei Tang, 2022, Frontiers in Immunology.

Novel mutations of TYK2 leading to divergent clinical phenotypes

Xiaodong Zhao, Xiao Du, Lina Zhou, 2021, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

CD8+ T‐cell senescence and skewed lymphocyte subsets in young Dyskeratosis Congenita patients with PARN and DKC1 mutations

Xiaodong Zhao, Xuemei Chen, Lina Zhou, 2020, Journal of clinical laboratory analysis.

Activated Phosphoinositide 3-Kinase δ Syndrome: a Large Pediatric Cohort from a Single Center in China

Xiaodong Zhao, Xuemei Chen, Lina Zhou, 2022, Journal of Clinical Immunology.

Molecular and Phenotypic Characterization of Nine Patients with STAT1 GOF Mutations in China

Xiaodong Zhao, Qin Zhao, Junfeng Wu, 2019, Journal of Clinical Immunology.

Clinical, genetic and immunological characteristics of 40 Chinese patients with CD40 ligand deficiency

Xiaodong Zhao, Xuemei Chen, Xiao Du, 2019, Scandinavian journal of immunology.

Novel biallelic TRNT1 mutations lead to atypical SIFD and multiple immune defects

Xiaodong Zhao, Qin Zhao, Xuemei Chen, 2020, Genes & diseases.

WASp Deficiency Selectively Affects the TCR Diversity of Different Memory T Cell Subsets in WAS Chimeric Mice

Xiaodong Zhao, Qin Zhao, Junfeng Wu, 2022, Frontiers in immunology.

Chinese a Nti鄄 Cancer a Ssociation

Hong-lin Xu, Hong Xu, X. Mo, 2022 .

A rare homozygous variant of MC2R gene identified in a Chinese family with familial glucocorticoid deficiency type 1: A case report

Furong Huang, Cheng Luo, T. Zeng, 2023, Frontiers in Endocrinology.

[A case report of BCL11B mutation induced neurodevelopmental disorder and literature review].

Y. An, Y. Wei, S. Yan, 2020, Zhonghua er ke za zhi = Chinese journal of pediatrics.