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349 related items for PubMed ID: 1363706

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.
    Bibi A, Messaoud T, Fattoum S.
    Hemoglobin; 2006; 30(2):175-81. PubMed ID: 16798642
    [Abstract] [Full Text] [Related]

  • 5. 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; 29(2):119-32. PubMed ID: 15921164
    [Abstract] [Full Text] [Related]

  • 6. Molecular spectrum of β-thalassemia mutations in the admixed Venezuelan population, and their linkage to β-globin gene haplotypes.
    Bravo-Urquiola M, Arends A, Gómez G, Montilla S, Gerard N, Chacin M, Berbar T, García O, García G, Velasquez D, Castillo O, Krishnamoorthy R.
    Hemoglobin; 2012; 36(3):209-18. PubMed ID: 22563936
    [Abstract] [Full Text] [Related]

  • 7. Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
    Colah R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Surve R, Subramaniam PG, Bondge N, Pujari K, Ghosh K, Mohanty D.
    Blood Cells Mol Dis; 2004; 33(2):153-7. PubMed ID: 15315795
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
    El-Gawhary S, El-Shafie S, Niazi M, Aziz M, El-Beshlawy A.
    Hemoglobin; 2007 Oct; 31(1):63-9. PubMed ID: 17365006
    [Abstract] [Full Text] [Related]

  • 10. [Molecular nature of beta-thalassemia in Tajikistan: a four base pair deletion in codons 41-42 of the beta-globin gene].
    Kolesnikova TN, Surin VL, Moliaka IuK, Luk'ianenko AV, Tagiev AF, Asanov AIu, Bobokhodzhaev ZM, Solov'ev GIa.
    Genetika; 1992 Nov; 28(11):28-33. PubMed ID: 1286798
    [Abstract] [Full Text] [Related]

  • 11. The molecular heterogeneity of beta-thalassemia in Greece.
    Boussiou M, Karababa P, Sinopoulou K, Tsaftaridis P, Plata E, Loutradi-Anagnostou A.
    Blood Cells Mol Dis; 2008 Nov; 40(3):317-9. PubMed ID: 18096416
    [Abstract] [Full Text] [Related]

  • 12. [Frequency of molecular alterations in heterozygous beta-thalassemia in southern Spain and their relation to the hematologic phenotype].
    Molina MA, Romero MJ, Abril E, Delgado I, Cano RM, Garrido F, de Pablos JM, Garrido ML.
    Sangre (Barc); 1994 Aug; 39(4):253-6. PubMed ID: 7985053
    [Abstract] [Full Text] [Related]

  • 13. [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
    [Abstract] [Full Text] [Related]

  • 14. [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
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Rapid detection of beta-Thalassemia alleles in Egypt using naturally or amplified created restriction sites and direct sequencing: a step in disease control.
    Hussein G, Fawzy M, Serafi TE, Ismail EF, Metwally DE, Saber MA, Giansily M, Schved JF, Pissard S, Martinez PA.
    Hemoglobin; 2007 Aug; 31(1):49-62. PubMed ID: 17365005
    [Abstract] [Full Text] [Related]

  • 17. Molecular basis of beta-thalassemia minor in Taiwan.
    Chang JG, Lin CP, Liu TC, Chiou SS, Chen PH, Lee LS, Chen TP.
    Int J Hematol; 1994 Jun; 59(4):267-72. PubMed ID: 8086620
    [Abstract] [Full Text] [Related]

  • 18. Genetic heterogeneity of Beta thalassemia in Lebanon reflects historic and recent population migration.
    Makhoul NJ, Wells RS, Kaspar H, Shbaklo H, Taher A, Chakar N, Zalloua PA.
    Ann Hum Genet; 2005 Jan; 69(Pt 1):55-66. PubMed ID: 15638828
    [Abstract] [Full Text] [Related]

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