Associated Papers
Genotypic Characterization of Thalassemia in Huadu District, Guangzhou, China: A Single-Center Retrospective Study.
Run G et al.
Hemoglobin, 2025
Noninvasive prenatal diagnosis for pregnancies at risk for β-thalassaemia: a retrospective study.
Lv W et al.
Bjog : an International Journal of Obstetrics and Gynaecology, 2021
Development of DNA controls for detection of β-thalassemia mutations commonly found in Asian.
Munkongdee T et al.
International Journal of Laboratory Hematology, 2020
Detection of three common mutations causing β-thalassemia by using a closed-tube multiplex PCR.
Jia X et al.
Experimental and Molecular Pathology, 2018
Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease.
Li A et al.
American Journal of Human Genetics, 2003
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