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Journal Abstract Search

181 related items for PubMed ID: 22239481

  • 21. Characterization of Hb Bart's Hydrops Fetalis Caused by - -SEA and a Large Novel α0-Thalassemia Deletion.
    He S, Li J, Huang P, Zhang S, Lin L, Zuo Y, Tian X, Zheng C, Qiu X, Chen B.
    Hemoglobin; 2018 Jan; 42(1):61-64. PubMed ID: 29493331
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  • 22. Hb Dapu (HBA2: c.52G > T): A Novel Nondeletional α-Thalassemia Mutation.
    Yang Y, Li DZ, He P.
    Hemoglobin; 2016 Aug; 40(4):264-6. PubMed ID: 27258683
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  • 23. α-Thalassemia syndromes in the United Arab Emirates.
    Baysal E.
    Hemoglobin; 2011 Aug; 35(5-6):574-80. PubMed ID: 22074123
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  • 24. Hb Bart's in cord blood: an accurate indicator of alpha-thalassemia.
    Rugless MJ, Fisher CA, Stephens AD, Amos RJ, Mohammed T, Old JM.
    Hemoglobin; 2006 Aug; 30(1):57-62. PubMed ID: 16540417
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  • 25. [Hb Bart's Quantitative Analysis in the Screening of α-Thalassemia].
    Yi S, Wang B, Li H, Zhang H, Song JP.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2021 Dec; 29(6):1903-1906. PubMed ID: 34893131
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  • 26. Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (- -SEA/) Deletion.
    Yang X, Yan JM, Li J, Xie XM, Zhou JY, Li Y, Li DZ.
    Hemoglobin; 2016 Sep; 40(5):353-355. PubMed ID: 27686733
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  • 28. Detection of Hb Constant Spring by a capillary electrophoresis method.
    Liao C, Zhou JY, Xie XM, Li J, Li R, Li DZ.
    Hemoglobin; 2010 Jan; 34(2):175-8. PubMed ID: 20353355
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  • 29. Detection of coinherited Hb H-Constant Spring/Paksé disease and Hb E by capillary electrophoresis and high performance liquid chromatography.
    Pornprasert S, Waneesorn J.
    Hemoglobin; 2013 Jan; 37(2):176-82. PubMed ID: 23234508
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  • 32. Molecular spectrum of alpha-thalassemia in Tunisia: epidemiology and detection at birth.
    Zorai A, Harteveld CL, Bakir A, Van Delft P, Falfoul A, Dellagi K, Abbes S, Giordano PC.
    Hemoglobin; 2002 Nov; 26(4):353-62. PubMed ID: 12484630
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  • 33. Simplified PGD of common determinants of haemoglobin Bart's hydrops fetalis syndrome using multiplex-microsatellite PCR.
    Wang W, Yap CH, Loh SF, Tan AS, Lim MN, Prasath EB, Chan ML, Tan WC, Jiang B, Yeo GH, Mathew J, Ho A, Ho SS, Wong PC, Choolani MA, Chong SS.
    Reprod Biomed Online; 2010 Nov; 21(5):642-8. PubMed ID: 20864413
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  • 34. Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland China.
    Jiang F, Xu LL, Chen GL, Zhou JY, Li J, Tang XW, Zuo LD, Li DZ.
    Hemoglobin; 2020 Mar; 44(2):86-88. PubMed ID: 32338097
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  • 35. Clinical features and molecular analysis in Thai patients with HbH disease.
    Laosombat V, Viprakasit V, Chotsampancharoen T, Wongchanchailert M, Khodchawan S, Chinchang W, Sattayasevana B.
    Ann Hematol; 2009 Dec; 88(12):1185-92. PubMed ID: 19390853
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  • 36. Hb Milano [α109(G16)Leu→Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the α1-Globin Gene in an Italian Family.
    Curcio C, Giannone V, Benzoni E, Cesaretti C, Ivaldi G.
    Hemoglobin; 2019 Jan; 43(1):4-6. PubMed ID: 31084368
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  • 39. Screening for co-existence of α-thalassemia in β-thalassemia and in HbE heterozygotes via an enzyme-linked immunosorbent assay for Hb Bart's and embryonic ζ-globin chain.
    Tatu T, Kiewkarnkha T, Khuntarak S, Khamrin S, Suwannasin S, Kasinrerk W.
    Int J Hematol; 2012 Apr; 95(4):386-93. PubMed ID: 22438184
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  • 40. Hb Westmead (HBA2: c.369C>G): Hematological Characteristics in Heterozygotes with and without α0-Thalassemia.
    Jiang F, Ju AP, Li J, Chen GL, Zhou JY, Tang XW, Zuo LD, Li DZ.
    Hemoglobin; 2020 May; 44(3):153-155. PubMed ID: 32436451
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