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198 related items for PubMed ID: 1724976

  • 21. Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassaemia due to a homozygosity for the IVS-I-6 (T-->C) mutation.
    Efremov DG, Dimovski AJ, Baysal E, Ye Z, Adekile AD, Ribeiro ML, Schiliro G, Altay C, Gürgey A, Efremov GD.
    Br J Haematol; 1994 Apr; 86(4):824-30. PubMed ID: 7522523
    [Abstract] [Full Text] [Related]

  • 22. Localisation of cis regulatory elements at the beta-globin locus: analysis of hybrid haplotype chromosomes.
    Ofori-Acquah SF, Lalloz MR, Layton DM.
    Biochem Biophys Res Commun; 1999 Jan 08; 254(1):181-7. PubMed ID: 9920754
    [Abstract] [Full Text] [Related]

  • 23. Sickle cell anemia in the Tunisian population: haplotyping and HB F expression.
    Abbes S, Fattoum S, Vidaud M, Goossens M, Rosa J.
    Hemoglobin; 1991 Jan 08; 15(1-2):1-9. PubMed ID: 1717403
    [Abstract] [Full Text] [Related]

  • 24. DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation.
    Elion J, Berg PE, Lapouméroulie C, Trabuchet G, Mittelman M, Krishnamoorthy R, Schechter AN, Labie D.
    Blood; 1992 Feb 01; 79(3):787-92. PubMed ID: 1346253
    [Abstract] [Full Text] [Related]

  • 25. Effect of alpha-thalassemia and beta-globin gene cluster haplotypes on the hematological and clinical features of sickle-cell anemia in Brazil.
    Figueiredo MS, Kerbauy J, Gonçalves MS, Arruda VR, Saad ST, Sonati MF, Stoming T, Costa FF.
    Am J Hematol; 1996 Oct 01; 53(2):72-6. PubMed ID: 8892730
    [Abstract] [Full Text] [Related]

  • 26. [Hemoglobin beta S haplotype in the Kebili region (southern Tunisia)].
    Frikha M, Fakhfakh F, Mseddi S, Gargouri J, Ghali L, Labiadh Z, Harrabi M, Souissi T, Ayadi H.
    Transfus Clin Biol; 1998 Apr 01; 5(2):166-72. PubMed ID: 9618841
    [Abstract] [Full Text] [Related]

  • 27. The relationship of the genetic heterogeneity of sickle cell gene to clinical manifestations.
    el-Hazmi MA.
    J Trop Pediatr; 1993 Feb 01; 39(1):23-9. PubMed ID: 8095305
    [Abstract] [Full Text] [Related]

  • 28. beta S haplotypes, alpha-globin gene status, and hematological data of sickle cell disease patients in Guadeloupe (F.W.I.).
    Kéclard L, Ollendorf V, Berchel C, Loret H, Mérault G.
    Hemoglobin; 1996 Feb 01; 20(1):63-74. PubMed ID: 8745433
    [Abstract] [Full Text] [Related]

  • 29. The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF level.
    Nagel RL, Rao SK, Dunda-Belkhodja O, Connolly MM, Fabry ME, Georges A, Krishnamoorthy R, Labie D.
    Blood; 1987 Apr 01; 69(4):1026-30. PubMed ID: 2435339
    [Abstract] [Full Text] [Related]

  • 30. The frequency of the gamma chain variant A gamma T in different populations, and its use in evaluating gamma gene expression in association with thalassemia.
    Huisman TH, Kutlar F, Nakatsuji T, Bruce-Tagoe A, Kilinç Y, Cauchi MN, Romero Garcia C.
    Hum Genet; 1985 Apr 01; 71(2):127-33. PubMed ID: 2412945
    [Abstract] [Full Text] [Related]

  • 31. Association of thalassaemia intermedia with a beta-globin gene haplotype.
    Thein SL, Wainscoat JS, Sampietro M, Old JM, Cappellini D, Fiorelli G, Modell B, Weatherall DJ.
    Br J Haematol; 1987 Mar 01; 65(3):367-73. PubMed ID: 2436649
    [Abstract] [Full Text] [Related]

  • 32. Sequence variations in the 5' flanking and IVS-II regions of the G gamma- and A gamma-globin genes of beta S chromosomes with five different haplotypes.
    Lanclos KD, Oner C, Dimovski AJ, Gu YC, Huisman TH.
    Blood; 1991 Jun 01; 77(11):2488-96. PubMed ID: 2039830
    [Abstract] [Full Text] [Related]

  • 33. Restriction mapping of βS locus among Tunisian sickle-cell patients.
    Imen M, Ikbel BM, Leila C, Fethi M, Amine Z, Mohamed B, Salem A.
    Am J Hum Biol; 2011 Jun 01; 23(6):815-9. PubMed ID: 21965081
    [Abstract] [Full Text] [Related]

  • 34. Xmn I polymorphism in the gamma-globin gene region among Saudis.
    el-Hazmi MA.
    Hum Hered; 1989 Jun 01; 39(1):12-9. PubMed ID: 2474486
    [Abstract] [Full Text] [Related]

  • 35. Sickle cell disease in the Kurdish population of northern Iraq.
    Al-Allawi NA, Jalal SD, Nerwey FF, Al-Sayan GO, Al-Zebari SS, Alshingaly AA, Markous RD, Jubrael JM, Hamamy H.
    Hemoglobin; 2012 Jun 01; 36(4):333-42. PubMed ID: 22686351
    [Abstract] [Full Text] [Related]

  • 36. Beta-globin gene haplotypes in the Saudi sickle cell anaemia patients.
    el-Hazmi MA.
    Hum Hered; 1990 Jun 01; 40(3):177-86. PubMed ID: 1973147
    [Abstract] [Full Text] [Related]

  • 37. Chronic inflammatory state in sickle cell anemia patients is associated with HBB(*)S haplotype.
    Bandeira IC, Rocha LB, Barbosa MC, Elias DB, Querioz JA, Freitas MV, Gonçalves RP.
    Cytokine; 2014 Feb 01; 65(2):217-21. PubMed ID: 24290434
    [Abstract] [Full Text] [Related]

  • 38. Dominant influence of gamma-globin promoter polymorphisms on fetal haemoglobin expression in sickle cell disease.
    Ofori-Acquah SF, Lalloz MR, Serjeant G, Layton DM.
    Cell Mol Biol (Noisy-le-grand); 2004 Feb 01; 50(1):35-42. PubMed ID: 15040425
    [Abstract] [Full Text] [Related]

  • 39. Association of the level of G gamma chain in the fetal hemoglobin of normal adults with specific haplotypes.
    Hattori Y, Kutlar F, Mosley CJ, Mayson SM, Huisman TH.
    Hemoglobin; 1986 Feb 01; 10(2):185-204. PubMed ID: 2420750
    [Abstract] [Full Text] [Related]

  • 40. Hematological effects of atypical and Cameroon beta-globin gene haplotypes in adult sickle cell anemia.
    Steinberg MH, Lu ZH, Nagel RL, Venkataramani S, Milner PF, Huey L, Safaya S, Rieder RF.
    Am J Hematol; 1998 Oct 01; 59(2):121-6. PubMed ID: 9766796
    [Abstract] [Full Text] [Related]

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