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Journal Abstract Search

181 related items for PubMed ID: 22239481

  • 1. Screening for common nondeletional α-thalassemias in Chinese newborns by determination of Hb Bart's using the Sebia Capillarys 2 electrophoresis system.
    Tang HS, Zhou JY, Xie XM, Li R, Liao C, Li DZ.
    Hemoglobin; 2012; 36(2):196-9. PubMed ID: 22239481
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  • 3. Newborn screening for Hb H disease by determination of Hb Bart's using the Sebia capillary electrophoresis system in southern China.
    Liao C, Zhou JY, Xie XM, Tang HS, Li R, Li DZ.
    Hemoglobin; 2014; 38(1):73-5. PubMed ID: 24229410
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  • 4. 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; 37(2):197-200. PubMed ID: 23390935
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  • 6. Analysis of Deletional Hb H Diseases in Samples with Hb A2-Hb H and Hb A2-Hb Bart's on Capillary Electrophoresis.
    Khongthai K, Ruengdit C, Panyasai S, Pornprasert S.
    Hemoglobin; 2019; 43(4-5):245-248. PubMed ID: 31687860
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  • 9. 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; 39(6):412-4. PubMed ID: 26212676
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  • 10. Hb J-Wenchang-Wuming [α11(A9)Lys→Gln (AAG>CAG) (α2 or α1)] compromises neonatal screening for α-thalassemia with the Sebia Capillarys2 electrophoresis system.
    Zhai YS, Tang HS, Li DZ.
    Hemoglobin; 2012; 36(4):395-8. PubMed ID: 22680346
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  • 11. Screening for Hb Constant Spring in the Guangdong Province, South China, using the Sebia capillary electrophoresis system.
    Liao C, Zhou JY, Xie XM, Li DZ.
    Hemoglobin; 2011; 35(1):87-90. PubMed ID: 21250886
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  • 12. Molecular screening of the Hbs Constant Spring (codon 142, TAA>CAA, α2) and Paksé (codon 142, TAA>TAT, α2) mutations in Thailand.
    Pichanun D, Munkongdee T, Klamchuen S, Butthep P, Winichagoon P, Fucharoen S, Svasti S.
    Hemoglobin; 2010; 34(6):582-6. PubMed ID: 21077767
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  • 13. 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; 32(5):454-61. PubMed ID: 18932070
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  • 16. Neonatal screening for alpha-thalassemia in southern Taiwan.
    Lin TM, Eng HL, Kuo PL, Wu HL.
    J Formos Med Assoc; 1992 Dec; 91(12):1213-5. PubMed ID: 1363647
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  • 17. Detection of α-thalassaemia in neonates on cord blood and dried blood spot samples by capillary electrophoresis.
    Alauddin H, Langa M, Mohd Yusoff M, Raja Sabudin RZA, Ithnin A, Abdul Razak NF, Sardi NH, Hussin NH.
    Malays J Pathol; 2017 Apr; 39(1):17-23. PubMed ID: 28413201
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  • 18. Phenotypic variability in a chinese family with nondeletional Hb H-Hb Quong Sze disease.
    Li J, Liao C, Zhou JY, Xie XM, Li R, Chen LH, Li DZ.
    Hemoglobin; 2011 Apr; 35(4):430-3. PubMed ID: 21797711
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