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Journal Abstract Search

149 related items for PubMed ID: 28406128

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  • 4. Impact of β(S)-globin haplotypes on oxidative stress in patients with sickle cell anemia in steady state.
    Carvalho-dos Santos BS, Dias-Elias DB, da Silva-Rocha LB, Cavalcante-Barbosa M, Pinheiro-Gonçalves R.
    Arch Med Res; 2012 Oct; 43(7):536-40. PubMed ID: 23085440
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  • 6. Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.
    Bean CJ, Boulet SL, Yang G, Payne AB, Ghaji N, Pyle ME, Hooper WC, Bhatnagar P, Keefer J, Barron-Casella EA, Casella JF, Debaun MR.
    Br J Haematol; 2013 Oct; 163(2):268-76. PubMed ID: 23952145
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  • 11. βS globin gene haplotype and the stroke risk among Egyptian children with sickle cell disease.
    Abou-Elew HH, Youssry I, Hefny S, Hashem RH, Fouad N, Zayed RA.
    Hematology; 2018 Jul; 23(6):362-367. PubMed ID: 29157167
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  • 14. Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.
    Koenig SC, Becirevic E, Hellberg MS, Li MY, So JC, Hankins JS, Ware RE, McMahon L, Steinberg MH, Luo HY, Chui DH.
    Am J Hematol; 2009 Sep; 84(9):603-6. PubMed ID: 19650141
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  • 17. β-globin gene cluster haplotypes in sickle cell patients from Panamá.
    Rusanova I, Cossio G, Moreno B, Javier Perea F, De Borace RG, Perea M, Escames G, Acuña-Castroviejo D.
    Am J Hum Biol; 2011 Sep; 23(3):377-80. PubMed ID: 21387457
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  • 19. 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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