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PUBMED FOR HANDHELDS

Journal Abstract Search


184 related items for PubMed ID: 24229410

  • 1. 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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  • 3. Neonatal screening for α-thalassemia by cord hemoglobin Barts: how effective is it?
    Wu MY, Xie XM, Li J, Li DZ.
    Int J Lab Hematol; 2015 Oct; 37(5):649-53. PubMed ID: 25955662
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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 Oct; 39(6):412-4. PubMed ID: 26212676
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  • 8. 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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  • 9. Cord blood screening for alpha-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: correlation with genotypes and hematologic parameters.
    Charoenkwan P, Taweephol R, Sirichotiyakul S, Tantiprabha W, Sae-Tung R, Suanta S, Sakdasirisathaporn P, Sanguansermsri T.
    Blood Cells Mol Dis; 2010 Jun 15; 45(1):53-7. PubMed ID: 20299254
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  • 11. Diagnostic applications of newborn screening for α-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spots.
    Jindatanmanusan P, Riolueang S, Glomglao W, Sukontharangsri Y, Chamnanvanakij S, Torcharus K, Viprakasit V.
    Ann Clin Biochem; 2014 Mar 15; 51(Pt 2):237-47. PubMed ID: 23901141
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  • 12. 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 15; 21(5):642-8. PubMed ID: 20864413
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  • 14. Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb Rotterdam): two novel alpha2 gene mutations associated with mild alpha-thalassemia found in the same family after newborn screening.
    Giordano PC, Cnossen MH, Joosten AM, Jansen CA, Hakvoort TE, Bakker-Verweij M, Arkesteijn SG, van Delft P, Waye JS, Bouva MJ, Harteveld CL.
    Hemoglobin; 2010 Nov 15; 34(4):354-65. PubMed ID: 20642333
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  • 18. Hemoglobin Lepore EF Bart's disease: a molecular, hematological, and diagnostic aspects.
    Chaibunruang A, Fucharoen G, Jetsrisuparb A, Fucharoen S.
    Ann Hematol; 2011 Nov 15; 90(11):1337-40. PubMed ID: 21302111
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  • 19. Four cases of Hb Q-H disease found in Southern China.
    Li D, Liao C, Xie X, Zhong H, Li J.
    Hemoglobin; 2007 Nov 15; 31(1):109-11. PubMed ID: 17365013
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  • 20. Early onset of fetal hydrops associated with the α-thalassemia - -(THAI) deletion.
    Yang Y, Li DZ.
    Hemoglobin; 2014 Nov 15; 38(6):431-4. PubMed ID: 25370866
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