The Association of Hemoglobin Knossos and Hemoglobin Lepore in an Algerian Patient
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630268408996971
Reference25 articles.
1. ‘Silent’ β-thalassaemia caused by a ‘silent’ β-chain mutant: the pathogenesis of a syndrome of thalassaemia intermedia
2. Structural study of hemoglobin Knossos, β27 (B9) Ala→Ser
3. The Diagnosis of Thalassemia Trait by Starch Block Electrophoresis of the Hemoglobin
4. THE FUSION OF TWO PEPTIDE CHAINS IN HEMOGLOBIN LEPORE AND ITS INTERPRETATION AS A GENETIC DELETION
5. Analysis of the β-δ-globin gene loci in normal and hb lepore DNA: Direct determination of gene linkage and intergene distance
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1. δ0-Thalassemia in cis of βKnossos globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tunisian patients;Clinical Chemistry and Laboratory Medicine;2012-01-01
2. Combination of Hb Knossos [Cod 27 (G-T)] and IVSII-745 (C-G) in a Turkish Patient with Beta-Thalassemia Major;Genetic Testing;2007-09
3. Compound Heterozygosity for Hb E and Hb Lepore-Hollandia in India; First Report and Potential Diagnostic Pitfalls;Hemoglobin;2005-01
4. Complex interactions of δβ hybrid haemoglobin (Hb Lepore-Hollandia) Hb E (β26 G→A ) and α+ thalassaemia in a Thai family;European Journal of Haematology;2002-02
5. Hb Arta [β45 (CD4) Phe→Cys]: a new unstable haemoglobin with reduced oxygen affinity in trans with β-thalassaemia;British Journal of Haematology;1995-11
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