Co-inherited β-thalassemia trait and HbH disease: clinical characteristics and interference in diagnosis of thalassemia by high-performance liquid chromatography
Author:
Publisher
Wiley
Subject
Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine
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1. Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations;Hemoglobin;2023-03-04
2. Advances in screening of thalassaemia;Clinica Chimica Acta;2022-09
3. Prenatal diagnosis of a rare β ‐thalassemia gene -90 (C>T) ( HBB : c.‐140 C>T) mutation associated with deletional Hb H disease (‐‐ SEA /‐ α 4.2 );Molecular Genetics & Genomic Medicine;2020-09-03
4. Analysis of Hb levels and degree of anemia in relation to genotype in 615 patients with hemoglobin H disease;Expert Review of Hematology;2020-08-11
5. α, β, δ and γ thalassaemias and related conditions;Haemoglobinopathy Diagnosis;2020-02-28
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