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Journal Abstract Search

144 related items for PubMed ID: 16370492

  • 1. High Hb A2 beta-thalassemia due to a 468 bp deletion in a patient with Hb S/beta-thalassemia.
    Patterson M, Walker L, Eng B, Waye JS.
    Hemoglobin; 2005; 29(4):293-5. PubMed ID: 16370492
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  • 2. Characterization of Two Novel Deletions Involving the 5' Region of the β-Globin Gene.
    Waye JS, Hanna M, Hohenadel BA, Nakamura L, Walker L, Eng B.
    Hemoglobin; 2017; 41(4-6):239-242. PubMed ID: 29182041
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  • 5. Filipino beta zero thalassaemia: a high Hb A2 beta zero thalassaemia resulting from a large deletion of the 5' beta globin gene region.
    Motum PI, Kearney A, Hamilton TJ, Trent RJ.
    J Med Genet; 1993 Mar; 30(3):240-4. PubMed ID: 7682618
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  • 6. 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 Mar; 35(4):406-10. PubMed ID: 21797706
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  • 7. Levels of Hb A2 in heterozygotes and homozygotes for beta-thalassemia mutations: influence of mutations in the CACCC and ATAAA motifs of the beta-globin gene promoter.
    Huisman TH.
    Acta Haematol; 1997 Mar; 98(4):187-94. PubMed ID: 9401495
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  • 8. Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.
    Jha AN, Mishra H, Verma HK, Pandey I, Lakkakula BVKS.
    Hemoglobin; 2018 Mar; 42(2):84-90. PubMed ID: 30200838
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  • 9. HbS/beta(del)-thalassemia associated with high levels of hemoglobins A2 and F in a Turkish family.
    Tadmouri GO, Yüksel L, Başak AN.
    Am J Hematol; 1998 Sep; 59(1):83-6. PubMed ID: 9723583
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  • 10. 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
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  • 11. Hb A1c Determination by Capillary Electrophoresis is an Efficient Method for Detecting β-Thalassemias and Hemoglobin Variants.
    Orts JA, Zúñiga Á, Bello Y, Fabregat AB, Vicente AI.
    Hemoglobin; 2016 Sep; 40(5):335-340. PubMed ID: 27535164
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  • 12. Analysis of the Genotypes in a Chinese Population with Increased Hb A2 and Low Hematological Indices.
    Jiang F, Chen GL, Li J, Zhou JY, Liao C, Li DZ.
    Hemoglobin; 2018 May; 42(3):154-158. PubMed ID: 30277083
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  • 13. Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish family.
    Gümrük F, Mergen H, Oner R, Ozcebe O, Sayinalp N, Oner C, Gürgey A, Altay C.
    Hemoglobin; 2000 Feb; 24(1):23-9. PubMed ID: 10722112
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  • 14. Hb A2-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A2-β-Thalassemia Trait.
    Chen GL, Huang LY, Zhou JY, Li DZ.
    Hemoglobin; 2017 Feb; 41(4-6):291-292. PubMed ID: 29251016
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  • 15. Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ)0-Thalassemia among Tunisian family.
    Kalai M, Moumni I, Ouragini H, Ben Fraj I, Mellouli F, Ouederni M, Chaouachi D, Boudriga I, Menif S.
    Ann Clin Biochem; 2023 Mar; 60(2):81-85. PubMed ID: 36214153
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  • 16. Genotype/Phenotype Correlation of β-Thalassemia in Syrian Patients: A Cross-Sectional Study.
    Shoujaa A, Moasses F, Mukhalalaty Y, Murad H, Al-Quobaili F.
    Hemoglobin; 2020 Jan; 44(1):42-46. PubMed ID: 31903828
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  • 17. Association of beta-thalassemia and Hb Q-Thailand resulting in a normal Hb A2 value.
    Liao C, Li J, Li D.
    Hemoglobin; 2008 Jan; 32(5):505-8. PubMed ID: 18932077
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  • 18. Normal Hb A2 β-thalassemia trait: frameshift mutation (HBB: c.187_251dup) in cis with the Hb A2' δ-globin gene missense mutation (HBD: c.49G>C).
    Waye JS, Eng B, Hellens L, Hohenadel BA, Nakamura LM, Walker L.
    Hemoglobin; 2013 Jan; 37(2):201-4. PubMed ID: 23398055
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  • 20. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
    Esteghamat F, Imanian H, Azarkeivan A, Pourfarzad F, Almadani N, Najmabadi H.
    Hemoglobin; 2007 Jan; 31(4):463-9. PubMed ID: 17994380
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