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Journal Abstract Search

225 related items for PubMed ID: 22962223

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  • 3. Hematological characterization of compound heterozygous hemoglobin Hope/E patients with and without alpha-thalassemia-1 SEA type deletion.
    Pornprasert S.
    Clin Lab; 2013; 59(9-10):1183-5. PubMed ID: 24273946
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  • 5. Phenotypic expression of hemoglobins A₂, E and F in various hemoglobin E related disorders.
    Sae-ung N, Srivorakun H, Fucharoen G, Yamsri S, Sanchaisuriya K, Fucharoen S.
    Blood Cells Mol Dis; 2012 Jan 15; 48(1):11-6. PubMed ID: 22014901
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  • 6. [Use of capillary electrophoresis to determine hemoglobin A2 in healthy adults and alpha- and beta-thalassemia carriers].
    Hua L, Li J, Liu ZY, Zhong HZ, Liao C, Xu XM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct 15; 20(5):421-4. PubMed ID: 14556197
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  • 7. 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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  • 8. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.
    Azma RZ, Othman A, Azman N, Alauddin H, Ithnin A, Yusof N, Razak NF, Sardi NH, Hussin NH.
    Malays J Pathol; 2012 Jun 15; 34(1):57-62. PubMed ID: 22870600
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  • 14. Epidemiology of Hemoglobinopathies in the Huzhou Region, Zhejiang Province, Southeast China.
    Ding ZY, Shen GS, Zhang S, He PY.
    Hemoglobin; 2016 Sep 15; 40(5):304-309. PubMed ID: 27615034
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  • 16. Hemoglobin Q-Thailand and its combinations with other forms of thalassemia or hemoglobinopathies in northern Thailand.
    Panyasai S, Pornprasert S.
    Clin Lab; 2014 Sep 15; 60(7):1099-103. PubMed ID: 25134377
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  • 20. Detection of Hb H disease caused by a novel mutation and --SEA deletion using capillary electrophoresis.
    Li Y, Liang L, Tian M, Qin T, Wu X.
    J Clin Lab Anal; 2019 Sep 15; 33(7):e22949. PubMed ID: 31199523
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