Different Forms of Hb H Disease in the Chinese
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630268808991638
Reference21 articles.
1. Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.
2. The molecular basis of alpha-thalassaemia in Thailand.
3. Organization of the ζ-α genes in Chinese
4. The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes
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1. A molecular study on the role of alpha-hemoglobin-stabilizing protein in hemoglobin H disease;Annals of Hematology;2017-03-23
2. Detection of Uncommon Deletions in Alpha-Thalassemia Using the PCR-Reverse Dot-Blot Method for Prenatal Diagnosis of Nondeletional Hemoglobin H Disease;Acta Haematologica;2010
3. Clinical features and molecular analysis in Thai patients with HbH disease;Annals of Hematology;2009-04-24
4. Variable Clinical Phenotypes of α-Thalassemia Syndromes;The Scientific World JOURNAL;2009
5. Thalassemia intermedia in HbH-CS disease with compound heterozygosity for .BETA.-thalassemia: Challenges in hemoglobin analysis and clinical diagnosis;Genes & Genetic Systems;2009
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