Associated Papers
Revealing silent alpha-thalassemia: characterization of novel HBA1 deletion and missense mutation in Tunisian families.
Amri Y et al.
Annals of Hematology, 2025
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-HBA1
In silico analysis of nonsynonymous single-nucleotide polymorphisms (nsSNPs) of the SMPX gene.
Arifuzzaman M et al.
Annals of Human Genetics, 2020
Application of flow cytometry-based genotyping for rapid detection of hemoglobin variants.
Aslanian S et al.
International Journal of Laboratory Hematology, 2007
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