Y. Zuo

发表

DNA methylation patterns of β-globin cluster in β-thalassemia patients

Diyu Chen, Cunyou Zhao, Xiuqin Bao, 2020, Clinical Epigenetics.

A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression.

Qiang Wu, Lihong Shi, Yuhua Ye, 2017, American journal of human genetics.

Common genetic polymorphisms at three loci affect HbF levels in β-thalassemia patients from Southern China.

Qi Yang, Sheng Yi, Jingsi Luo, 2016, Blood cells, molecules & diseases.

A novel 223 kb deletion in the beta‐globin gene cluster was identified in a Chinese thalassemia major patient

Decheng Cai, Xiangmin Xu, X. Shang, 2019, International journal of laboratory hematology.

First Identification of the 3.5 kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the β-Globin Gene Cluster in a Chinese Family

X. Qiu, Sheng He, Chenguang Zheng, 2018, Hemoglobin.

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.

Reference intervals for erythrocyte parameters and hemoglobin electrophoresis parameters for young children in Guangxi

Xiangmin Xu, Jingsi Luo, Sheng He, 2022, International journal of laboratory hematology.

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 prevalence and molecular characterization of (δβ)0‐thalassemia and hereditary persistence of fetal hemoglobin in the Chinese Zhuang population

Hongwei Wei, X. Qiu, Shang Yi, 2017, Journal of clinical laboratory analysis.

A novel missense mutation in F9 gene causes hemophilia B in a family with clinical variability.

Meng Li, Z. Qin, Qinle Zhang, 2020, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

A novel variant of osteogenesis imperfecta type IV and low serum phosphorus level caused by a Val94Asp mutation in COL1A1

Z. Qin, Qinle Zhang, Qi Yang, 2018, Molecular medicine reports.

Molecular Characterization of α- and β-Thalassaemia Among Children From 1 to 10 Years of Age in Guangxi, A Multi-Ethnic Region in Southern China

Chaofan Zhou, Hongwei Wei, Shang Yi, 2021, Frontiers in Pediatrics.

[Study on the characteristics of major birth defects in 1.69 million cases of fetus in Guangxi Zhuang Autonomous Region].

B. Dong, X. Qiu, J. Wei, 2019, Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi.

Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia.

Dali Li, Yafeng Li, Yukio Nakamura, 2021, American Journal of Human Genetics.

DNA methylation patterns of β-globin cluster in β-thalassemia patients

Diyu Chen, Cunyou Zhao, Xiuqin Bao, 2020, Clinical epigenetics.