Associated Papers
Prediction the Occurrence of Thalassemia With Hematological Phenotype by Diagnosis of Abnormal HbA1c.
Wan Y et al.
Journal of Clinical Laboratory Analysis, 2024
39317177 (PubMed )
Supplement: JCLA-38-e25104-s001.xlsx › Mutations
Spectrum of HBB gene mutations among 696 β-thalassemia patients and carriers in Southern Vietnam.
Xinh PT et al.
Molecular Biology Reports, 2022
Prenatal Genetic Counseling in a Chinese Pregnant Woman With Rare Thalassemia: A Case Report.
Zhong L et al.
Frontiers in Genetics, 2021
Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population.
Hamid M et al.
Hemoglobin, 2020
Next-generation sequencing improves molecular epidemiological characterization of thalassemia in Chenzhou Region, P.R. China.
Zhang H et al.
Journal of Clinical Laboratory Analysis, 2019
HBB: c.316-125A>G and HBB: c.316-42delC: Phenotypic Evaluations of Two Rare Changes in the Second Intron of the HBB Gene.
Vinciguerra M et al.
Hemoglobin, 0
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