Associated Papers
A new unstable haemoglobin, Hb Alger, causes a transfusion-dependent anaemia in early childhood.
Bouazizi S et al.
British Journal of Haematology, 2025
Mutation Analysis of Exon 1 in the Hemoglobin Subunit Beta (HBB) Gene in Beta-Thalassemia.
Kumar KS et al.
Cureus, 2024
Early Onset of Severe Anemia Caused by Hb Calgary (HBB: C.194G > T): Another Case Report.
Jiang H et al.
Hemoglobin, 2024
Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies.
Tamana S et al.
Elife, 2022
36453528 (PubMed )
Supplement: elife-79713-supp2.xlsx › Input-Full_dataset
Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a β-Thalassemia Major Phenotype.
Martin G et al.
Hemoglobin, 2021
Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
Henderson SJ et al.
Hemoglobin, 2016
Mutational spectrum of delta-globin gene in the Portuguese population.
Morgado A et al.
European Journal of Haematology, 2007
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