Associated Papers
Relevance of Next-Generation Sequencing in the Diagnosis of Thalassemia and Hemoglobinopathies: The Experience of Four Italian Diagnostic Hubs.
Selvatici R et al.
Genes, 2024
Heterozygosity of the Complex Corfu δ0β+ Thalassemic Allele (HBD Deletion and HBB:c.92+5G>A) Revisited
Kattamis C et al.
Biology, 2022
HBB mutations and HbA2 level: Escaping the carrier screening programs.
Sharifi A et al.
Clinical Case Reports, 2021
Molecular Characterization of δ-Thalassemia in Iran.
Kordafshari A et al.
Hemoglobin, 2016
Molecular update of β-thalassemia mutations in the Syrian population: identification of rare β-thalassemia mutations.
Jarjour RA et al.
Hemoglobin, 2014
Characterization of three novel delta chain hemoglobin variants and two delta-thalassemia alleles.
Frischknecht H et al.
Hemoglobin, 2010
Select a paper to view details