Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience
- 1 December 2000
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 111 (3) , 915-923
- https://doi.org/10.1111/j.1365-2141.2000.02448.x
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Rapid and Accurate Quantitation of Hb Bart's and Hb H Using Weak Cation Exchange High Performance Liquid Chromatography: Correlation with the α-Thalassemia GenotypeHemoglobin, 1999
- Interaction of an α+-Thalassemia Deletion with Either a Highly Unstable α-Globin Variant (α2, Codon 59, GGC→GAC) or a Nondeletional α-Thalassemia Mutation (AATAA→AATAAG): Comparison of Phenotypes Illustrating “Dominant” α-ThalassemiaHemoglobin, 1999
- Hb Aghia Sophia [α62(E11)Val→0 (α1)], an “In-Frame” Deletion Causing α-ThalassemiaHemoglobin, 1999
- The Thalassemia Repository (Ninth Edition; Part II)Hemoglobin, 1998
- An α-Thalassemic Hemoglobinopathy: Homozygosity for the Hb Agrinio α2-Globin Chain VariantHemoglobin, 1998
- Chapter 2 Hemolytic anemias due to hemoglobinopathiesMolecular Aspects of Medicine, 1996
- The interaction of α° thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy HBritish Journal of Haematology, 1996
- A base substitution (T→C) in codon 29 of the α2-globin gene causes α thalassaemiaBritish Journal of Haematology, 1993
- Hb H Disease Caused by a Homozygosity for the AATAAA→ AATAAG Mutation in the Polyadenylation Site of the α2-Globin Gene: Hematological ObservationsActa Haematologica, 1992
- Compensatory increase in alpha 1-globin gene expression in individuals heterozygous for the alpha-thalassemia-2 deletion.Journal of Clinical Investigation, 1985