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Journal Abstract Search

251 related items for PubMed ID: 20854126

  • 1. Severe β-thalassemia intermedia in a compound heterozygous patient for the -30 (T>A) β(+)-thalassemia mutation and the δ(0)β(+)-Senegalese deletion.
    Griffon C, Joly P, Sénéchal A, Philit F, Francina A.
    Hemoglobin; 2010; 34(5):505-8. PubMed ID: 20854126
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  • 2. Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion.
    Waye JS, Eng B, Got T, Hanna M, Hohenadel BA, Nakamura LM, Walker L.
    Hemoglobin; 2015; 39(5):368-70. PubMed ID: 26154945
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  • 4. Molecular characterization of a Chinese pedigree with beta-thalassemia intermedia.
    Huang G, Jiang WL, Rong KB, Li YX, Luo XL, Meng JX, Yu XY.
    Hemoglobin; 2010 Jan; 34(2):179-83. PubMed ID: 20353356
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  • 6. The rare codon 24 (T>A) (beta+) mutation in association with the common codon 39 (C> T) (beta0) mutation causes transfusion-dependent beta-thalassemia in a Moroccan patient.
    Agouti I, Bennani M, Levy N, Giordano P, Badens C.
    Hemoglobin; 2009 Jan; 33(2):150-4. PubMed ID: 19373592
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  • 8. 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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  • 9. HbA2-Partinico or delta(A2)Pro-->Thr, a new genetic variation in the delta-globin gene in cis to the beta(+) thal IVS-I-110 G>A, and the heterogeneity of delta-globin alleles in double heterozygotes for beta- and delta-globin gene defects.
    Lacerra G, Scarano C, Musollino G, Testa R, Prezioso R, Caruso DG, Lagona LF, Medulla E, Friscia MG, Gaudiano C, Carestia C.
    Ann Hematol; 2010 Feb; 89(2):127-34. PubMed ID: 19609526
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  • 12. New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG].
    Phylipsen M, Harteveld CL, de Metz M, Gallivan MV, Arkesteijn SG, Luo HY, Chui DH, Giordano PC.
    Hemoglobin; 2010 Feb; 34(5):445-50. PubMed ID: 20854118
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  • 17. Comparison of two known chromosomal rearrangements in the δβ-globin complex with identical DNA breakpoints but causing different Hb A(2) levels.
    Saller E, Moradkhani K, Dutly F, Vinatier I, Préhu C, Frischknecht H, Goossens M.
    Hemoglobin; 2012 Feb; 36(2):177-82. PubMed ID: 22273484
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  • 20. A novel mutation of -50 (G-->A) in the direct repeat element of the beta-globin gene identified in a patient with severe beta-thalassemia.
    Li DZ, Liao C, Xie XM, Zhou JY.
    Ann Hematol; 2009 Nov; 88(11):1149-50. PubMed ID: 19290524
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