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Journal Abstract Search

277 related items for PubMed ID: 20854114

  • 21. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene.
    Panyasai S, Jaiping K, Pornprasert S.
    Hemoglobin; 2015; 39(4):292-5. PubMed ID: 26029792
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  • 23. Hb Charlieu [alpha106(G13)Leu-->Pro (alpha1)]: a new phenotypically silent hemoglobin variant associated with a mild alpha-thalassemia phenotype.
    Joly P, Szymanowicz A, Neyron MJ, Zine A, Wajcman H, Francina A.
    Hemoglobin; 2010; 34(4):366-73. PubMed ID: 20642334
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  • 29. 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; 34(5):445-50. PubMed ID: 20854118
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  • 31. 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; 36(2):177-82. PubMed ID: 22273484
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  • 33. Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations.
    Kasmi C, Amri Y, Hadj-Fredj S, Oueslati S, Dabboussi M, Mahjoub R, Hammami S, Aljane I, Mami FB, Jamoussi H, Messaoud T, Bibi A.
    Mol Biol Rep; 2021 Aug; 48(8):5923-5933. PubMed ID: 34341901
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  • 40. Characterization of three novel delta chain hemoglobin variants and two delta-thalassemia alleles.
    Frischknecht H, Troxler H, Dutly F, Walker L, Hohenadel BA, Eng B, Waye JS.
    Hemoglobin; 2010 Aug; 34(4):374-82. PubMed ID: 20642335
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