The Corfu δβ thalassaemia mutation in Greece: haematological phenotype and prevalence
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1991.tb04537.x/fullpdf
Reference20 articles.
1. Molecular characterization of a novel form of (A ) -thalassemia, deletion with a 3' breakpoint close to those of HPFH-3 and HPFH-4: insights for a common regulatory mechanism
2. Nonrandom association of polymorphic restriction sites in the -globin gene cluster
3. DNA polymorphism and molecular pathology of the human globin gene clusters
4. Four new haplotypes observed in Algerian ?-thalassemia patients
5. Deletion delta-thalassemia: the 7.2 kb deletion of Corfu delta beta- thalassemia in a non-beta-thalassemia chromosome [letter]
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1. Severe clinical picture in a cohort of six Brazilian children with hemoglobin Sβ-thalassemia IVS-I-5 G>A;Blood Cells, Molecules, and Diseases;2024-01
2. Heterozygosity of the Complex Corfu δ0β+ Thalassemic Allele (HBD Deletion and HBB:c.92+5G>A) Revisited;Biology;2022-03-11
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4. The Molecular Basis of -Thalassemia;Cold Spring Harbor Perspectives in Medicine;2013-05-01
5. Characterization of three new deletions in the β-globin gene cluster during a screening survey in two French urban areas;Clinica Chimica Acta;2013-01
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