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Journal Abstract Search

241 related items for PubMed ID: 25682598

  • 1. Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region.
    Amid A, Cheong M, Eng B, Hanna M, Hohenadel BA, Nakamura LM, Walker L, Odame I, Kirby-Allen M, Waye JS.
    Haematologica; 2015 May; 100(5):e166-8. PubMed ID: 25682598
    [No Abstract] [Full Text] [Related]

  • 2. Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotype.
    Daniel Y, Hill K, Inusa B, Thein SL, Howard J.
    Hemoglobin; 2011 May; 35(4):406-10. PubMed ID: 21797706
    [Abstract] [Full Text] [Related]

  • 3. A novel deletion/insertion caused by a replication error in the β-globin gene locus control region.
    Joly P, Lacan P, Garcia C, Meley R, Pondarré C, Francina A.
    Hemoglobin; 2011 May; 35(4):316-22. PubMed ID: 21797698
    [Abstract] [Full Text] [Related]

  • 4. β-globin gene cluster haplotypes in a cohort of 221 children with sickle cell anemia or Sβ⁰-thalassemia and their association with clinical and hematological features.
    Belisário AR, Martins ML, Brito AM, Rodrigues CV, Silva CM, Viana MB.
    Acta Haematol; 2010 May; 124(3):162-70. PubMed ID: 20938172
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Splice Acceptor Mutation [HBB:c.93-2A > T] in a Patient with Hb S/β0-Thalassemia.
    Waye JS, Hanna M, Nakamura L, Walker L, Eng B, Nfonsam LE.
    Hemoglobin; 2024 Mar; 48(2):116-117. PubMed ID: 38360540
    [Abstract] [Full Text] [Related]

  • 7. Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics.
    Belisário AR, Carneiro-Proietti AB, Sabino EC, Araújo A, Loureiro P, Máximo C, Flor-Park MV, Rodrigues DDOW, Ozahata MC, McClure C, Mota RA, Gomes Moura IC, Custer B, Kelly S, Recipient Epidemiology and Donor Evaluation Study (REDS-III) International Component Brazil.
    Hemoglobin; 2020 Jan; 44(1):1-9. PubMed ID: 32172616
    [Abstract] [Full Text] [Related]

  • 8. Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
    Muszlak M, Pissard S, Badens C, Chamouine A, Maillard O, Thuret I.
    Hemoglobin; 2015 Jan; 39(3):156-61. PubMed ID: 25806420
    [Abstract] [Full Text] [Related]

  • 9. Heterozygosity for deletion of hypersensitive site 3 in the human locus control region has an unexpected minor effect on red cell phenotype.
    Nieto JM, Villegas A, De La Fuente-Gonzalo F, González FA, Ropero P.
    J Hum Genet; 2014 Oct; 59(10):585-7. PubMed ID: 25186056
    [Abstract] [Full Text] [Related]

  • 10. Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.
    Murad H, Moassas F, Jarjour R, Mukhalalaty Y, Al-Achkar W.
    Hemoglobin; 2014 Oct; 38(6):390-3. PubMed ID: 25405916
    [Abstract] [Full Text] [Related]

  • 11. Microsatellite and single nucleotide polymorphisms in the β-globin locus control region-hypersensitive Site 2: SPECIFICITY of Tunisian βs chromosomes.
    Ben Mustapha M, Moumni I, Zorai A, Douzi K, Ghanem A, Abbes S.
    Hemoglobin; 2012 Oct; 36(6):533-44. PubMed ID: 23101664
    [Abstract] [Full Text] [Related]

  • 12. A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization.
    Singha K, Fucharoen G, Hama A, Fucharoen S.
    Clin Biochem; 2015 Jul; 48(10-11):703-8. PubMed ID: 25866400
    [Abstract] [Full Text] [Related]

  • 13. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion.
    Andersson BA, Wering ME, Luo HY, Basran RK, Steinberg MH, Smith HP, Chui DH.
    Eur J Haematol; 2007 Jan; 78(1):82-5. PubMed ID: 17038017
    [Abstract] [Full Text] [Related]

  • 14. Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients.
    Azarkeivan A, Cohan N, Niazkar HR, Azizi A, Rad F.
    Hemoglobin; 2020 Mar; 44(2):109-112. PubMed ID: 32370567
    [Abstract] [Full Text] [Related]

  • 15. Silent β-thalassemia mutations at -101 (C>T) and -71 (C>T) and their coinheritance with the sickle cell mutation in Bahrain.
    Al Moamen NJ, Mahdi F, Salman E, Ahmed T, Abbas R, Al Arrayed S, Sanad H, Ahmed AA.
    Hemoglobin; 2013 Mar; 37(4):369-77. PubMed ID: 23586372
    [Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of β-thalassemia and other hemoglobinopathies in southwestern Turkey.
    Mendilcioglu I, Yakut S, Keser I, Simsek M, Yesilipek A, Bagci G, Luleci G.
    Hemoglobin; 2011 Mar; 35(1):47-55. PubMed ID: 21250881
    [Abstract] [Full Text] [Related]

  • 17. 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 Mar; 36(4):333-42. PubMed ID: 22686351
    [Abstract] [Full Text] [Related]

  • 18. HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype-phenotype correlation.
    Notarangelo LD, Agostini A, Casale M, Samperi P, Arcioni F, Gorello P, Perrotta S, Masera N, Barone A, Bertoni E, Bonetti E, Burnelli R, Casini T, Del Vecchio GC, Filippini B, Giona F, Giordano P, Gorio C, Marchina E, Nardi M, Petrone A, Colombatti R, Sainati L, Russo G.
    Eur J Haematol; 2020 Mar; 104(3):214-222. PubMed ID: 31788855
    [Abstract] [Full Text] [Related]

  • 19. A novel β-globin gene mutation HBB.c.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC.
    Edison ES, Sathya M, Rajkumar SV, Nair SC, Srivastava A, Shaji RV.
    Int J Lab Hematol; 2012 Oct; 34(5):556-8. PubMed ID: 22471768
    [Abstract] [Full Text] [Related]

  • 20. Coinheritance of Hb S [β6(A3)Glu→Val, GAG>GTG] with β0-thalassemia codon 17 (A>T) in a Thai patient.
    Pornprasert S, Panyasai S, Kongthai K, Treesuwan K.
    Hemoglobin; 2012 Oct; 36(3):265-9. PubMed ID: 22471390
    [Abstract] [Full Text] [Related]

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