Haplotypes and levels of fetal hemoglobin andGγ toAγ ratios in mediterranean patients with thalassemia minor and major
Author:
Publisher
Wiley
Subject
Hematology
Reference30 articles.
1. Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster
2. Five haplotypes in Black β-thalassaemia heterozygotes: three are associated with high and two with lowGγ values in fetal haemoglobin
3. beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site.
4. Four new haplotypes observed in Algerian ?-thalassemia patients
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1. Genetic factors involved in human Gγ and Aγ globin gene expression;European Journal of Haematology;2009-04-24
2. Hb Jambol: A New Hyperunstable Hemoglobin Causing Severe Hemolytic Anemia;Acta Haematologica;2006-11-08
3. Hb Stara Zagora: A New Hyper-Unstable Hemoglobin Causing Severe Hemolytic Anemia;Hemoglobin;2005-01
4. Genetic heterogeneity of β-thalassemia in southeast sicily;American Journal of Hematology;1995-01
5. Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with β-thalassaemia due to a homozygosity for the IVS-I-6 (T→C) mutation;British Journal of Haematology;1994-04
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