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Journal Abstract Search

514 related items for PubMed ID: 30843739

  • 21.
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  • 22. Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation.
    Ozkinay F, Onay H, Karaca E, Arslan E, Erturk B, Ece Solmaz A, Tekin IM, Cogulu O, Aydinok Y, Vergin C.
    Hemoglobin; 2015; 39(4):230-4. PubMed ID: 26076395
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  • 23. Molecular spectrum of β-thalassemia mutations in the admixed Venezuelan population, and their linkage to β-globin gene haplotypes.
    Bravo-Urquiola M, Arends A, Gómez G, Montilla S, Gerard N, Chacin M, Berbar T, García O, García G, Velasquez D, Castillo O, Krishnamoorthy R.
    Hemoglobin; 2012; 36(3):209-18. PubMed ID: 22563936
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  • 24. IVS-II-16 (G>C) (HBB: c.315+16G>C) or IVS-II-666 (C>T) (HBB: c.316-185C>T) Mutations Trigger an Hb S (HBB: c.20A>T)/β+-Thalassemia Phenotype in an Hb S Trait Patient.
    Uçucu S, Karabıyık T, Azik FM.
    Hemoglobin; 2021 Jul; 45(4):225-227. PubMed ID: 34396882
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  • 25. Molecular basis of β-thalassemia in the western province of Saudi Arabia: identification of rare β-thalassemia mutations.
    Abuzenadah AM, Hussein IM, Damanhouri GA, A-Sayes FM, Gari MA, Chaudhary AG, Zaher GF, Al-Attas A, Al-Qahtani MH.
    Hemoglobin; 2011 Jul; 35(4):346-57. PubMed ID: 21797702
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  • 26.
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  • 28. Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2.
    Nuinoon M, Thipthara O, Fucharoen S.
    Hemoglobin; 2019 Jan; 43(1):52-55. PubMed ID: 31106603
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  • 29. The phenomena of balanced effect between α-globin gene and of β-globin gene.
    Zhong L, Gan X, Xu L, Liang C, Xie Y, Lin W, Chen P, Liu M.
    BMC Med Genet; 2018 Aug 17; 19(1):145. PubMed ID: 30119651
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  • 30.
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  • 32. Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs.
    Adekile AD, Gu LH, Baysal E, Haider MZ, al-Fuzae L, Aboobacker KC, al-Rashied A, Huisman TH.
    Acta Haematol; 1994 Aug 17; 92(4):176-81. PubMed ID: 7701914
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  • 33. A Triple-Heterozygous β-Thalassemia Patient Demonstrated an Unusual Electrophoresis Pattern Due to a Novel β0 Mutation [an IVS-II-654 (C>T) mutation with a Hb Zürich-Langstrasse (HBB: c.151A>T) mutation in cis].
    Liao J, Li Q, Ling LQ, Liu CN, Huang XB, Zhou J.
    Hemoglobin; 2022 Jul 17; 46(4):249-252. PubMed ID: 35575165
    [Abstract] [Full Text] [Related]

  • 34. Mild Thalassemia Intermedia Due to Interaction of δβ-Thalassemia with Triplicated α-Globin Genes.
    Payán-Pernía S, Bernal Noguera S, Rojas Rodríguez E, Serra Ferrer M, Remacha Sevilla ÁF.
    Hemoglobin; 2020 Jul 17; 44(4):294-296. PubMed ID: 32693657
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  • 35. First Detection of a Splice Site β-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family.
    Chen B, Huang P, Yi S, Chen Q, Tang Y, Zhang Q, He S.
    Hemoglobin; 2015 Jul 17; 39(3):207-8. PubMed ID: 25856402
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  • 36.
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  • 38. Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn, HBB: c.[79G>A;198G>C]): A Novel β-Thalassemic Hemoglobin Variant.
    Satthakarn S, Boonmee S, Panyasai S.
    Hemoglobin; 2020 Nov 17; 44(6):385-390. PubMed ID: 33222574
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  • 39.
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  • 40.
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