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Journal Abstract Search

216 related items for PubMed ID: 9045354

  • 21. 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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  • 22. 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; 40(3):317-9. PubMed ID: 18096416
    [Abstract] [Full Text] [Related]

  • 23. [Diagnostic strategy of beta-thalassemic mutation in a Tunisian family, application in prenatal diagnosis].
    Khelil AH, Laradi S, Ferchichi S, Carion N, Béjaoui M, Saad A, Chaieb A, Miled A, Ben Chibani J, Perrin P.
    Ann Biol Clin (Paris); 2003; 61(2):229-33. PubMed ID: 12702481
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  • 24. First Spanish case of thalassemia major due to a compound heterozygosity for the IVS-II-848 (C --> A) and codon 39 (C --> T) mutations of the beta-globin gene.
    Ropero P, Villegas A, Muñoz J, Briceño O, Mora A, Salvador M, Polo M, González FA.
    Hemoglobin; 2006; 30(1):15-21. PubMed ID: 16540410
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  • 25. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
    Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK.
    Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
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  • 27. Detection of beta-thalassemia carrier by direct analysis of beta-globin gene lesions.
    Pao CC, Lin CY, Tang GC, Sun CF, Hsieh TT.
    Biochem Biophys Res Commun; 1993 Mar 31; 191(3):1118-23. PubMed ID: 8466489
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  • 32. Rapid and direct detection of the most frequent Mediterranean beta-thalassemic mutations by multiplex allele-specific enzymatic amplification.
    Bienvenu T, Sebillon P, Labie D, Kaplan JC, Beldjord C.
    Hum Biol; 1992 Feb 31; 64(1):107-13. PubMed ID: 1582644
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  • 35. 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 31; 59(4):267-72. PubMed ID: 8086620
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  • 36. A pilot beta-thalassaemia screening program in the Albanian population for a health planning program.
    Baghernajad-Salehi L, D'Apice MR, Babameto-Laku A, Biancolella M, Mitre A, Russo S, Di Daniele N, Sangiuolo F, Mokini V, Novelli G.
    Acta Haematol; 2009 Jun 31; 121(4):234-8. PubMed ID: 19556751
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  • 37. Spectrum of beta-thalassemia mutations in North Indian states: a beta-thalassemia trait with two mutations in cis.
    Chakrabarti P, Gupta R, Mishra A, Rai M, Singh VP, Dash D.
    Clin Biochem; 2005 Jun 31; 38(6):576-8. PubMed ID: 15885239
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  • 38. Molecular analysis of unknown beta-globin gene mutations using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique and its application in Thai families with beta-thalassemias and beta-globin variants.
    Chinchang W, Viprakasit V, Pung-Amritt P, Tanphaichitr VS, Yenchitsomanus PT.
    Clin Biochem; 2005 Nov 31; 38(11):987-96. PubMed ID: 16139831
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  • 39. β-Thalassemia mutations in the Kurdish population of northeastern Iraq.
    Jalal SD, Al-Allawi NA, Bayat N, Imanian H, Najmabadi H, Faraj A.
    Hemoglobin; 2010 Nov 31; 34(5):469-76. PubMed ID: 20854121
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  • 40. Screening of beta-thalassemia mutations by PCR and ASO analysis in an Italian population of mixed geographic origin.
    Alfarano A, Gottardi E, Serra A, Piga A, Mandrino M, Mazza U, Camaschella C.
    Haematologica; 1990 Nov 31; 75(6):506-9. PubMed ID: 2098291
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