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Journal Abstract Search


122 related items for PubMed ID: 2408656

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  • 3. Fetal haemoglobin production and the sickle gene in the oases of Eastern Saudi Arabia.
    Pembrey ME, Wood WG, Weatherall DJ, Perrine RP.
    Br J Haematol; 1978 Nov; 40(3):415-29. PubMed ID: 749927
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  • 4. Analysis of hemoglobin F production in Saudi Arabian families with sickle cell anemia.
    Miller BA, Salameh M, Ahmed M, Olivieri N, Antognetti G, Orkin SH, Huisman TH, Nathan DG.
    Blood; 1987 Sep; 70(3):716-20. PubMed ID: 2441778
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  • 6. High fetal hemoglobin production in sickle cell anemia in the eastern province of Saudi Arabia is genetically determined.
    Miller BA, Salameh M, Ahmed M, Wainscoat J, Antognetti G, Orkin S, Weatherall D, Nathan DG.
    Blood; 1986 May; 67(5):1404-10. PubMed ID: 2421808
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  • 7. Interaction of deletional alpha-thalassaemia with sickle cell beta-thalassaemia and its influence on foetal haemoglobin expression.
    Vidaud-Raphanaud D, Krishnamoorthy R, Schaison G, Labie D.
    Ann Genet; 1988 May; 31(1):32-5. PubMed ID: 2451466
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  • 8. Hematological observations on Arabian SS patients with a homozygosity or heterozygosity for a beta S chromosome with haplotype #31.
    Kutlar A, Hattori Y, Bakioglu I, Kutlar F, Kamel K, Huisman TH.
    Hemoglobin; 1985 May; 9(6):545-57. PubMed ID: 2419279
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  • 9. Raised Hb F levels in sickle cell disease are caused by a determinant linked to the beta globin gene cluster.
    Kulozik AE, Thein SL, Kar BC, Wainscoat JS, Serjeant GR, Weatherall DJ.
    Prog Clin Biol Res; 1987 May; 251():427-39. PubMed ID: 2448811
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  • 10. Molecular analysis of the high-hemoglobin-F phenotype in Saudi Arabian sickle cell anemia.
    Miller BA, Olivieri N, Salameh M, Ahmed M, Antognetti G, Huisman TH, Nathan DG, Orkin SH.
    N Engl J Med; 1987 Jan 29; 316(5):244-50. PubMed ID: 2432426
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  • 16. Fetal haemoglobin level--effect of gender, age and haemoglobin disorders.
    el-Hazmi MA, Warsy AS, Addar MH, Babae Z.
    Mol Cell Biochem; 1994 Jun 29; 135(2):181-6. PubMed ID: 7530809
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  • 18. Homozygous sickle cell disease in Uganda and Jamaica a comparison of Bantu and Benin haplotypes.
    Ndugwa C, Higgs D, Fisher C, Hambleton I, Mason K, Serjeant BE, Serjeant GR.
    West Indian Med J; 2012 Oct 29; 61(7):684-91. PubMed ID: 23620965
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  • 19. Xmn I polymorphism in the gamma-globin gene region among Saudis.
    el-Hazmi MA.
    Hum Hered; 1989 Oct 29; 39(1):12-9. PubMed ID: 2474486
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  • 20. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
    Adeyemo T, Ojewunmi O, Oyetunji A.
    Pan Afr Med J; 2014 Oct 29; 18():71. PubMed ID: 25400838
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