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Journal Abstract Search

277 related items for PubMed ID: 9640613

  • 1. Analysis of beta-thalassemia mutations and beta-locus control region hypersensitive sites 2, 3 and 4 in southern Thailand.
    Sriroongrueng W, Schleiemacher E, Panich V, Nopparatana C, Saechan V, Laosombat V, Pornpatkul M, Fukumaki Y.
    Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():120-7. PubMed ID: 9640613
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  • 2. The spectrum of beta-thalassemia mutations in southern Thailand.
    Nopparatana C, Panich V, Saechan V, Sriroongrueng V, Nopparatana C, Rungjeadpha J, Pornpatkul M, Laosombat V, Fukumaki Y.
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():229-34. PubMed ID: 8629112
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  • 3. Molecular heterogeneity of beta-thalassemia in Thailand.
    Fukumaki Y, Fucharoen S, Fucharoen G, Okamoto N, Ichinose M, Jetsrisuparb A, Sriroongrueng W, Nopparatana C, Laosombat V, Panich V.
    Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():14-21. PubMed ID: 1363706
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  • 4. Spectrum of beta-thalassemia mutations and their association with allelic sequence polymorphisms at the beta-globin gene cluster in an Eastern Indian population.
    Kukreti R, Dash D, E VK, Chakravarty S, Das SK, De M, Talukder G.
    Am J Hematol; 2002 Aug; 70(4):269-77. PubMed ID: 12210807
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  • 6. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM, El-Khatib FF, Ayesh S.
    Hemoglobin; 2005 Aug; 29(2):119-32. PubMed ID: 15921164
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  • 11. Molecular analysis of beta-thalassemia in South Vietnam.
    Svasti S, Hieu TM, Munkongdee T, Winichagoon P, Van Be T, Van Binh T, Fucharoen S.
    Am J Hematol; 2002 Oct; 71(2):85-8. PubMed ID: 12353305
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  • 12. [Most frequent beta-thalassemia mutations in the Argentinian population].
    Varela V, Abreu S, Rossetti LC, Targovnik H.
    Sangre (Barc); 1996 Apr; 41(2):137-40. PubMed ID: 9045354
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  • 13. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].
    Indrák K, Divoký V, Brabec V, Indráková J, Svobodová M, Huisman TH.
    Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425
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  • 14. Homogeneity of beta(0)-thalassemia codon 17 (A-->T) alleles in Northern Thailand using a direct DNA sequencing method.
    Sanguansermsri P, Shimbhu D, Wongvilairat R, Saetung R, Sanguansermsri T.
    J Med Assoc Thai; 2004 Aug; 87(8):883-6. PubMed ID: 15471290
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  • 15. Molecular analysis of β-thalassemia patients: first identification of mutations HBB:c.93-2A>G and HBB:c.114G>A in Brazil.
    Fernandes AC, Shimmoto MM, Furuzawa GK, Vicari P, Figueiredo MS.
    Hemoglobin; 2011 Aug; 35(4):358-66. PubMed ID: 21797703
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