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Journal Abstract Search

263 related items for PubMed ID: 25523870

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  • 3. First Case of a Compound Heterozygosity for Two Nondeletional α-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze.
    Zhou JY, Yan JM, Li J, Li DZ.
    Hemoglobin; 2016 Jun; 40(3):210-2. PubMed ID: 26956449
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  • 4. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS, He J, Zhang J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
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  • 5. The Prevalence and Spectrum of α-Thalassemia in Guizhou Province of South China.
    Huang SW, Xu Y, Liu XM, Zhou M, Li GF, An BQ, Su L, Wu X, Lin J.
    Hemoglobin; 2015 Feb; 39(4):260-3. PubMed ID: 26193976
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  • 6. Prevention of Hb Bart's (γ4) Disease Associated with the - -(THAI) α(0)-Thalassemia Deletion in Mainland China.
    Li DZ, Li Y, Li J, Li SC, Li R.
    Hemoglobin; 2015 Feb; 39(6):412-4. PubMed ID: 26212676
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  • 9. Hb Constant Spring [alpha 142, Term-->Gln (TAA>CAA in alpha2)] in the alpha-thalassemia of anemic patients in Myanmar.
    Ne-Win, Harano K, Harano T, Kyaw-Shwe, Aye-Aye-Myint, Khin-Thander-Aye, Okada S.
    Hemoglobin; 2008 Feb; 32(5):454-61. PubMed ID: 18932070
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  • 13. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.
    Li D, Liao C, Li J, Xie X, Huang Y, Zhong H.
    Haematologica; 2006 May; 91(5):649-51. PubMed ID: 16627247
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  • 15. Molecular characterization of Hb H disease in southern Thailand.
    Nittayaboon K, Nopparatana C.
    Int J Hematol; 2018 Oct; 108(4):384-389. PubMed ID: 30006733
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  • 18. Detection of Hb Constant Spring [α142, Term→Gln, TAA>CAA (α2)] in heterozygotes combined with β-thalassemia.
    Li YQ, Li R, Li DZ.
    Hemoglobin; 2013 Oct; 37(2):197-200. PubMed ID: 23390935
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