Haemoglobin F (HbF) levels in sickle-cell anaemia patients homozygous for the Bantu haplotype
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1999.tb01128.x/fullpdf
Reference12 articles.
1. Fetal hemoglobin levels and βs globin haplotypes in an Indian population with sickle-cell disease;Kulozik;Blood,1987
2. Clinical features of sickle-cell disease in Eastern Saudi Arabia children;El Mouzan;Am J Haematol Oncol,1990
3. A profile of sickle-cell disease in Nigeria;Akinyanju;Ann NY Acad Sci,1989
4. High fetal hemoglobin production in sickle-cell anemia in Eastern Province of Saudi Arabia is genetically determined;Miller;Blood,1986
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1. Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia;Annals of Hematology;2019-09-02
2. Correlation between the Lactate Dehydrogenase Levels with Laboratory Variables in the Clinical Severity of Sickle Cell Anemia in Congolese Patients;PLOS ONE;2015-05-06
3. Foetal haemoglobin and disease severity in sickle cell anaemia patients in Kampala Uganda;BMC Blood Disorders;2012-09-07
4. Clinical and molecular characteristics of sickle cell anemia in the northeast of Brazil;Genetics and Molecular Biology;2008
5. Subclassification of HbS syndrome: is it necessary?;Clinical & Laboratory Haematology;2003-11-27
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