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Journal Abstract Search

341 related items for PubMed ID: 29484903

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  • 2. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM.
    Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043
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  • 3. Hemoglobin Q-Thailand and its combinations with other forms of thalassemia or hemoglobinopathies in northern Thailand.
    Panyasai S, Pornprasert S.
    Clin Lab; 2014; 60(7):1099-103. PubMed ID: 25134377
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  • 4. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy.
    Sanchaisuriya K, Chunpanich S, Fucharoen S, Fucharoen G, Sanchaisuriya P, Changtrakun Y.
    Eur J Haematol; 2005 Mar; 74(3):221-7. PubMed ID: 15693792
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  • 5. 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 Mar; 37(2):176-82. PubMed ID: 23234508
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  • 6. Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family.
    He S, Qin Q, Lin L, Chen Q, Yi S, Wei H, Du J, Zheng C, Qiu X, Chen B.
    Hemoglobin; 2017 Jan; 41(1):68-72. PubMed ID: 28475397
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  • 7. Hemoglobin Q-Thailand related disorders: origin, molecular, hematological and diagnostic aspects.
    Singsanan S, Karnpean R, Fucharoen G, Sanchaisuriya K, Sae-Ung N, Fucharoen S.
    Blood Cells Mol Dis; 2010 Oct 15; 45(3):210-4. PubMed ID: 20615730
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  • 8. Detection of Hb Constant Spring (HBA2: c.427T>C) Heterozygotes in Combination with β-Thalassemia or Hb E Trait by Capillary Electrophoresis.
    Pornprasert S, Saoboontan S, Punyamung M.
    Hemoglobin; 2015 Oct 15; 39(3):211-5. PubMed ID: 25884994
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  • 13. Molecular lesion frequency of hemoglobin gene disorders in Taiwan.
    Liu SC, Peng CT, Lin TH, Wang SJ, Shih MC, Tien N, Chang CC, Lu JJ, Lin CY.
    Hemoglobin; 2011 Oct 15; 35(3):228-36. PubMed ID: 21599435
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  • 15. Coinheritance of Hb A2-Melbourne (HBD: c.130G>A) and Hb E (HBB: c.79G>A) in Laos and Simultaneous High Resolution Melt Detection of Hb A2-Melbourne and Hb A2-Lampang (HBD: c.142G>A) in a Single Tube.
    Jomoui W, Panichchob P, Rujirachaivej P, Panyasai S, Tepakhan W.
    Hemoglobin; 2019 May 15; 43(3):214-217. PubMed ID: 31450984
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  • 17. Five hemoglobin variants in a double heterozygote for α- and β-globin chain defects.
    Singha K, Fucharoen G, Fucharoen S.
    Acta Haematol; 2014 May 15; 131(2):71-5. PubMed ID: 24081021
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