Associated Papers
Saliva Sample-Based Non-Invasive Carrier Screening for Spinal Muscular Atrophy, Hereditary Hearing Loss, and Thalassemia in 13,926 Women of Reproductive Age From South Zhejiang.
Xu C et al.
Molecular Genetics & Genomic Medicine, 2025
High accuracy of single-molecule real-time sequencing in detecting a rare α-globin fusion gene in carrier screening population.
Zhou QM et al.
Annals of Human Genetics, 2023
Molecular prevalence of HBB-associated hemoglobinopathy among reproductive-age adults and the prenatal diagnosis in Jiangxi Province, southern central China.
Luo H et al.
Frontiers in Genetics, 2022
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.
He S et al.
Frontiers in Pediatrics, 2021
Development of a genomic DNA reference material panel for thalassemia genetic testing.
Yin Z et al.
International Journal of Laboratory Hematology, 2020
Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene HBA2: c.1A>G Mutation.
Chen X et al.
Hemoglobin, 2020
Gene spectrum analysis of thalassemia for people residing in northern China.
Yang Z et al.
Bmc Medical Genetics, 2019
Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive Program.
Jiang F et al.
Hemoglobin, 0
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