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Journal Abstract Search

122 related items for PubMed ID: 2408656

  • 21.
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  • 22. Beta-globin gene haplotypes in the Saudi sickle cell anaemia patients.
    el-Hazmi MA.
    Hum Hered; 1990; 40(3):177-86. PubMed ID: 1973147
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  • 24. Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene cluster.
    Boyer SH, Dover GJ, Serjeant GR, Smith KD, Antonarakis SE, Embury SH, Margolet L, Noyes AN, Boyer ML, Bias WB.
    Blood; 1984 Nov; 64(5):1053-8. PubMed ID: 6207872
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  • 26. Post-natal decline of fetal haemoglobin in homozygous sickle cell disease: relationship to parenteral Hb F levels.
    Mason KP, Grandison Y, Hayes RJ, Serjeant BE, Serjeant GR, Vaidya S, Wood WG.
    Br J Haematol; 1982 Nov; 52(3):455-63. PubMed ID: 6181802
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  • 27. Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.
    Labie D, Pagnier J, Lapoumeroulie C, Rouabhi F, Dunda-Belkhodja O, Chardin P, Beldjord C, Wajcman H, Fabry ME, Nagel RL.
    Proc Natl Acad Sci U S A; 1985 Apr; 82(7):2111-4. PubMed ID: 2580306
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  • 32. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.
    Adekile A, Kutlar F, McKie K, Addington A, Elam D, Holley L, Clair B, Kutlar A.
    Eur J Haematol; 2005 Aug; 75(2):150-5. PubMed ID: 16004608
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  • 33. Phenotypic variation in sickle cell disease: the role of beta globin haplotype, alpha thalassemia, and fetal hemoglobin in HbSS.
    Serjeant GR.
    Expert Rev Hematol; 2022 Feb; 15(2):107-116. PubMed ID: 35143361
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  • 34. DNA haplotypes in Africans and West Indians with sickle cell anaemia or SC disease.
    Konstantopoulos K, Vulliamy T, Swirsky D, Reeves JD, Kaeda J, Luzzatto L.
    Gene Geogr; 1996 Apr; 10(1):19-24. PubMed ID: 8913718
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  • 38. Ocular findings in Saudi Arabian patients with sickle cell disease.
    al-Hazzaa S, Bird AC, Kulozik A, Serjeant BE, Serjeant GR, Thomas P, Padmos A.
    Br J Ophthalmol; 1995 May; 79(5):457-61. PubMed ID: 7612559
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  • 39. Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.
    Alsultan A, Alabdulaali MK, Griffin PJ, Alsuliman AM, Ghabbour HA, Sebastiani P, Albuali WH, Al-Ali AK, Chui DH, Steinberg MH.
    Br J Haematol; 2014 Feb; 164(4):597-604. PubMed ID: 24224700
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  • 40. Relationship of haemoglobin F and alpha thalassaemia to severity of sickle-cell anaemia in the Eastern Province of Saudi Arabia.
    Al-Awamy BH, Niazi GA, el-Mouzan MI, Altorki MT, Naeem MA.
    Ann Trop Paediatr; 1986 Dec; 6(4):261-5. PubMed ID: 2435232
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