Li Lin

发表

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

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

A High Proportion of Novel ACAN Mutations and Their Prevalence in a Large Cohort of Chinese Short Stature Children

Yiping Shen, J. Chen, Xiaoping Luo, 2021, The Journal of clinical endocrinology and metabolism.

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.

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.

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.

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.

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.

A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis.

Decheng Cai, X. Shang, Min Liang, 2020, Gene.

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.

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

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