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Journal Abstract Search

593 related items for PubMed ID: 24471655

  • 1.
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  • 2. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
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  • 3. 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 Nov; 37(2):201-4. PubMed ID: 23398055
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  • 6. Hb A2 Hong Kong - A novel δ-globin variant in a Chinese family masks the diagnosis of β-thalassemia trait.
    So CC, Chan AY, Luo HY, Verhovsek M, Chui DH, Ling SC, Chan LC.
    Hemoglobin; 2011 Nov; 35(2):162-5. PubMed ID: 21417575
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  • 7. 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 Nov; 34(5):445-50. PubMed ID: 20854118
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  • 11. A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg,HBD: C.139G > A].
    Lin HM, Liang L, Cai YJ, Zheng LH, Qin QP, Li YQ.
    Hemoglobin; 2024 Mar; 48(2):121-124. PubMed ID: 38450437
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  • 12. Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand.
    Panyasai S, Pornprasert S.
    Hemoglobin; 2020 May; 44(3):179-183. PubMed ID: 32482156
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  • 14. First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.
    Amirian A, Karimipoor M, Jafarinejad M, Taghavi M, Kordafshari A, Fathi Azar S, Mohammadi MS, Zeinali S.
    Arch Iran Med; 2011 Jan; 14(1):8-11. PubMed ID: 21194254
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  • 15. Molecular Characterization of δ-Thalassemia in Iran.
    Kordafshari A, Amirian A, Zeinali S, Valaei A, Maryami F, Karimipoor M.
    Hemoglobin; 2016 Jan; 40(1):44-7. PubMed ID: 26754299
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  • 16. A Case Report of Compound Heterozygosity for β0/β+-Thalassemia Resulting from under Diagnosed β-Thalassemia Found in a Hb A'2 Sample.
    Intasai N, Phasit A, Panyasai S, Pornprasert S.
    Hemoglobin; 2019 Jan; 43(1):63-65. PubMed ID: 31037981
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  • 17. Comprehensive spectrum of the β-Thalassemia mutations in Khuzestan, southwest Iran.
    Galehdari H, Salehi B, Azmoun S, Keikhaei B, Zandian KM, Pedram M.
    Hemoglobin; 2010 Jan; 34(5):461-8. PubMed ID: 20854120
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  • 19. First description of a Hb A2 variant in Thailand. Identification of Hb A2-Melbourne [δ43(CD2)Glu→Lys] in Thai individuals.
    Chaibunruang A, Fucharoen G, Fucharoen S.
    Hemoglobin; 2012 Jan; 36(1):80-4. PubMed ID: 21967556
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  • 20. Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in Cis.
    Colaco S, Trivedi A, Colah RB, Ghosh K, Nadkarni AH.
    Hemoglobin; 2014 Jan; 38(1):24-7. PubMed ID: 24200152
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