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Journal Abstract Search

284 related items for PubMed ID: 31903828

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  • 4. 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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  • 5. Genotype-Phenotype Correlation of β-Thalassemia in Malaysian Population: Toward Effective Genetic Counseling.
    Abdullah UYH, Ibrahim HM, Mahmud NB, Salleh MZ, Teh LK, Noorizhab MNFB, Zilfalil BA, Jassim HM, Wilairat P, Fucharoen S.
    Hemoglobin; 2020 May; 44(3):184-189. PubMed ID: 32586164
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  • 10. A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (HBB: c.27delG) in a Bangladeshi Family Acquired De Novo.
    Hasan KN, Sufian A, Mazumder AK, Khaleque MA, Rahman M, Akhteruzzaman S.
    Hemoglobin; 2019 May; 43(3):162-165. PubMed ID: 31339392
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  • 12. A Novel Human β-Globin Gene Variant [Hb London-Ontario, HBB: c.332T>G] is Associated with Transfusion-Dependent Anemia in a Patient with a Hemoglobin Electrophoresis Pattern Consistent with β-Thalassemia Trait.
    Bienz MN, Hsia C, Waye JS, Bode M, Solh Z.
    Hemoglobin; 2019 Mar; 43(2):129-131. PubMed ID: 31246535
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  • 14. Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics.
    Belisário AR, Carneiro-Proietti AB, Sabino EC, Araújo A, Loureiro P, Máximo C, Flor-Park MV, Rodrigues DDOW, Ozahata MC, McClure C, Mota RA, Gomes Moura IC, Custer B, Kelly S, Recipient Epidemiology and Donor Evaluation Study (REDS-III) International Component Brazil.
    Hemoglobin; 2020 Jan; 44(1):1-9. PubMed ID: 32172616
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  • 15. Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran.
    Sajadpour Z, Amini-Farsani Z, Motovali-Bashi M, Yadollahi M, Khosravi-Farsani N.
    Hemoglobin; 2020 Jan; 44(1):27-30. PubMed ID: 31899996
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  • 16. Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln; HBB: c.442T>C)] on the β-Globin Gene.
    Su Q, Chen S, Wu L, Tian R, Yang X, Huang X, Chen Y, Peng Z, Chen J.
    Hemoglobin; 2019 Jan; 43(1):7-11. PubMed ID: 31084366
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  • 18. 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 Jan; 38(2):88-90. PubMed ID: 24471655
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  • 20. 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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