Chenguang Zheng

发表

James Cheng, Han Yang, Hongzhi Chen, 2022, Proceedings of the VLDB Endowment.

The association between four SNPs (rs7482144, rs4671393, rs28384513 and rs4895441) and fetal hemoglobin levels in Chinese Zhuang β-thalassemia intermedia patients.

Ze Yang, Hongwei Wei, Shang Yi, 2017, Blood cells, molecules & diseases.

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.

Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients

Guojian Li, Hongwei Wei, Sheng Yi, 2016, Hemoglobin.

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.

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.

Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern China.

Shaoke Chen, Shang Yi, Sheng He, 2017, Gene.

Positive Rate of Noninvasive Prenatal Screening for Pregnancies with Fetal Congenital Heart Disease and Its Impact on Pregnancy Outcome

Yiping Shen, Xiao-Xian Tian, Hongwei Wei, 2020 .

Molecular characterization of α- and β-thalassemia in the Yulin region of Southern China.

X. Qiu, Shang Yi, Yi Liang, 2018, Gene.

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.

Etiology and Perinatal Outcome of Nonimmune Hydrops Fetalis in Southern China

Xiao-Xian Tian, Hongwei Wei, X. Qiu, 2017, American Journal of Perinatology Reports.

Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family

Guojian Li, Hongwei Wei, X. Qiu, 2016, Hemoglobin.

Hb H Hydrops Fetalis Syndrome Caused by Association of the − −SEA Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family

Xiao-Xian Tian, Shaoke Chen, Qiang Zhang, 2015, Hemoglobin.

Deletion and Hb Constant Spring (HBA2: c.427T4C) Mutation in a Chinese Family

Xiao-Xian Tian, Shaoke Chen, Qiang Zhang, 2015 .

Prevention and control of Hb Bart's disease in Guangxi Zhuang Autonomous Region, China.

Shaoke Chen, Qiang Zhang, Sheng He, 2014, European journal of obstetrics, gynecology, and reproductive biology.

Prenatal diagnosis of β-thalassemia in Guangxi Zhuang Autonomous Region, China

Qiang Zhang, Sheng He, Chenguang Zheng, 2013, Archives of Gynecology and Obstetrics.

First Detection of a Splice Acceptor Site β-Thalassemia Mutation: IVS-I-130 (HBB: c.93-1G > C) in a Chinese Patient

Shaoke Chen, Qiang Zhang, Sheng He, 2015, Hemoglobin.

Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family

X. Qiu, Shang Yi, Sheng He, 2017, Hemoglobin.

A Novel Mutation of the α2-Globin Gene Causing α+-Thalassemia: Hb Nanning (HBA2: c.369_370delinsGA)

Guojian Li, Hongwei Wei, X. Qiu, 2017, Hemoglobin.

Human STEAP3 mutations with no phenotypic red cell changes.

Wanjun Zhou, Li Lin, N. Mohandas, 2016, Blood.

Antineoplastic effect of calycosin on osteosarcoma through inducing apoptosis showing in vitro and in vivo investigations.

Yu Ye, Yun Liu, G. Bi, 2014, Experimental and molecular pathology.