Haplotypes and α globin gene analyses in sickle cell anaemia patients from Kenya
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1987.tb02267.x/fullpdf
Reference33 articles.
1. The distribution of the sickle-cell trait in East Africa and elsewhere, and its apparent relationship to the incidence of subtertian malaria
2. Sickle cell anaemia among Eti-Turks: haematological, clinical and genetic observations
3. Origin of the beta S-globin gene in blacks: the contribution of recurrent mutation or gene conversion or both.
4. Five adults with mild sickle cell anemia share a βs chromosome with the same haplotype
5. GγAγ(δβ)°-thalassaemia and a new form of γ globin gene triplication identified in the Yugoslavian population
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1. ACS in children with sickle cell anaemia in Uganda: prevalence, presentation and aetiology;British Journal of Haematology;2018-08-20
2. Sickle cell disease in Africa: an overview of the integrated approach to health, research, education and advocacy in Tanzania, 2004-2016;British Journal of Haematology;2017-03-14
3. Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift β-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2];Hemoglobin;2017-03-04
4. The effects of old and recent migration waves in the distribution of HBB*S globin gene haplotypes;Genetics and Molecular Biology;2016-10-03
5. Alpha thalassemia among sickle cell anaemia patients in Kampala, Uganda;African Health Sciences;2015-05-28
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