Qiuli Chen

发表

Identification of novel mutations in the HbF repressor gene BCL11A in patients with autism and intelligence disabilities

Jinchen Li, T. Cai, Zhouwen He, 2017, American journal of 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.

The correlation between neonatal vitamin D levels and the risk of childhood asthma attacks

Jinjie Zhou, L. Zhong, Lingyun Yang, 2021, Translational pediatrics.

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.

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.

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

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

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 cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature

Z. Qin, Jiasun Su, Weiliang Lu, 2019, Molecular Cytogenetics.

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.

Early onset horizontal gaze palsy and progressive scoliosis due to a noncanonical splicing‐site variant and a missense variant in the ROBO3 gene

Z. Qin, Qinle Zhang, Shang Yi, 2023, Molecular genetics & genomic medicine.

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.