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Journal Abstract Search

167 related items for PubMed ID: 34341901

  • 21. A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A].
    Moumni I, Zorai A, Mahjoub S, Mosbahi I, Chaouechi D, Benromdhane N, Abbes S.
    Hemoglobin; 2014; 38(2):88-90. PubMed ID: 24471655
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  • 22. 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; 37(2):201-4. PubMed ID: 23398055
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  • 23. Haemoglobinopathies that occur with decreased HbA2 levels: a gene mutation set involving the δ gene at a Spanish centre.
    Villegas A, González FA, Nieto JM, de la Fuente-Gonzalo F, Martínez R, Torrejón MJ, Ropero P.
    J Clin Pathol; 2017 Jan; 70(1):75-80. PubMed ID: 27387985
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  • 24. Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A2 Levels.
    Satthakarn S, Panyasai S, Pornprasert S.
    Hemoglobin; 2020 Sep; 44(5):349-353. PubMed ID: 33023363
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  • 30. A study of δ-globin gene mutations in the UK population: identification of three novel variants and development of a novel DNA test for Hb A'2.
    Khalil MS, Marouf S, Element D, Timbs A, Gallienne A, Schuh A, Old JM, Henderson S.
    Hemoglobin; 2014 Sep; 38(3):201-6. PubMed ID: 24601842
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  • 32. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.
    Prakobkaew N, Fucharoen S, Fuchareon G, Siriratmanawong N.
    Eur J Haematol; 2014 Jan; 92(1):73-9. PubMed ID: 24112054
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  • 33. Five novel globin gene mutations identified in five Chinese families by next-generation sequencing.
    Zhang J, Xie M, Peng Z, Zhou X, Zhao T, Jin C, Yan Y, Zeng X, Li D, Zhang Y, Su J, Feng N, He J, Yao X, Lv T, Zhu B.
    Mol Genet Genomic Med; 2021 Dec; 9(12):e1835. PubMed ID: 34708592
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  • 35. Rare hemoglobin variants in Tunisian population.
    Zorai A, Moumni I, Mosbahi I, Douzi K, Chaouachi D, Guemira F, Abbes S.
    Int J Lab Hematol; 2015 Apr; 37(2):148-54. PubMed ID: 24905386
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  • 36. δ-Globin Chain Variants Associated with Decreased Hb A2 Levels: A National Reference Laboratory Experience.
    Rets AV, Reading NS, Agarwal AM.
    Hemoglobin; 2020 Nov; 44(6):438-441. PubMed ID: 33054450
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  • 39. Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter.
    Coleman MB, Adams JG, Plonczynski MW, Harrell AH, Walker AM, Fairbanks V, Steinberg MH.
    Am J Med Sci; 1992 Aug; 304(2):73-8. PubMed ID: 1380206
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