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Journal Abstract Search

429 related items for PubMed ID: 15224373

  • 1. High frequency of deletional alpha-thalassemia in beta-thalassemia trait: implications for genetic counseling.
    Panigrahi I, Rafeeq PH, Choudhry VP, Saxena R.
    Am J Hematol; 2004 Jul; 76(3):297-9. PubMed ID: 15224373
    [Abstract] [Full Text] [Related]

  • 2. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand.
    Yamsri S, Sanchaisuriya K, Fucharoen G, Sae-Ung N, Fucharoen S.
    Blood Cells Mol Dis; 2011 Aug 15; 47(2):120-4. PubMed ID: 21664157
    [Abstract] [Full Text] [Related]

  • 3. Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.
    Galanello R, Perseu L, Perra C, Maccioni L, Barella S, Longinotti M, Cao A, Cazzola M.
    Br J Haematol; 2004 Dec 15; 127(5):604-6. PubMed ID: 15566365
    [Abstract] [Full Text] [Related]

  • 4. [Genetic screening for alpha-thalassemia deletional determinants by GapPCR method].
    Katol J, Takao M, Ideguchi H, Sawada H, Kawashima H, Ono J.
    Rinsho Byori; 2006 Nov 15; 54(11):1095-100. PubMed ID: 17240829
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 79(5):417-21. PubMed ID: 17900295
    [Abstract] [Full Text] [Related]

  • 6. Delta-thalassemia in Cyprus.
    Pavlou E, Phylactides M, Kyrri A, Kalogerou E, Makariou C, Georgiou I, Kleanthous M.
    Hemoglobin; 2006 Nov 15; 30(4):455-62. PubMed ID: 16987800
    [Abstract] [Full Text] [Related]

  • 7. [Genetic diagnosis of alpha and beta thalassemia dual heterozygote].
    Zeng R, Yu S, Hu B.
    Zhonghua Xue Ye Xue Za Zhi; 1998 Oct 15; 19(10):525-7. PubMed ID: 11189497
    [Abstract] [Full Text] [Related]

  • 8. Molecular characterization of deletional forms of beta-thalassemia in Taiwan.
    Peng CT, Liu SC, Chiou SS, Kuo PL, Shih MC, Chang JY, Chang JG.
    Ann Hematol; 2003 Jan 15; 82(1):33-6. PubMed ID: 12574962
    [Abstract] [Full Text] [Related]

  • 9. Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicine.
    Akerman BR, Fujiwara TM, Lancaster GA, Morgan K, Scriver CR.
    Am J Med Genet; 1990 May 15; 36(1):76-84. PubMed ID: 2333910
    [Abstract] [Full Text] [Related]

  • 10. [The prevalence of beta-thalassemia heterozygotes compound alpha-thalassemia in Guangdong district].
    Han J, Zeng R, Hu B.
    Zhonghua Xue Ye Xue Za Zhi; 2001 Oct 15; 22(10):514-6. PubMed ID: 11769674
    [Abstract] [Full Text] [Related]

  • 11. Extended molecular spectrum of beta- and alpha-thalassemia in Oman.
    Hassan SM, Hamza N, Jaffer Al-Lawatiya F, Jaffer Mohammed A, Harteveld CL, Rajab A, Giordano PC.
    Hemoglobin; 2010 Jan 15; 34(2):127-34. PubMed ID: 20353347
    [Abstract] [Full Text] [Related]

  • 12. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
    Panyasai S, Fucharoen S, Surapot S, Fucharoen G, Sanchaisuriya K.
    Haematologica; 2004 Jul 15; 89(7):777-81. PubMed ID: 15257928
    [Abstract] [Full Text] [Related]

  • 13. Prevalence and genotypes of alpha- and beta-thalassemia carriers in Hong Kong -- implications for population screening.
    Lau YL, Chan LC, Chan YY, Ha SY, Yeung CY, Waye JS, Chui DH.
    N Engl J Med; 1997 May 01; 336(18):1298-301. PubMed ID: 9113933
    [Abstract] [Full Text] [Related]

  • 14. Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermedia.
    Papachatzopoulou A, Kourakli A, Makropoulou P, Kakagianne T, Sgourou A, Papadakis M, Athanassiadou A.
    Eur J Haematol; 2006 Apr 01; 76(4):322-30. PubMed ID: 16519704
    [Abstract] [Full Text] [Related]

  • 15. A novel 33.3 kb deletion (- -KOL) in the alpha-globin gene cluster: a brief report on deletional alpha-thalassaemia in the heterogeneous eastern Indian population.
    Sarkar AA, Banerjee S, Chandra S, Ghosh M, Banerjee D, Choudhury MD, Das M, Dasgupta UB.
    Br J Haematol; 2005 Aug 01; 130(3):454-7. PubMed ID: 16042697
    [Abstract] [Full Text] [Related]

  • 16. Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin gene.
    Traeger-Synodinos J, Papassotiriou I, Vrettou C, Skarmoutsou C, Stamoulakatou A, Kanavakis E.
    Haematologica; 2001 Apr 01; 86(4):363-7. PubMed ID: 11325640
    [Abstract] [Full Text] [Related]

  • 17. Development of a quantitative real-time PCR assay for detection of unknown alpha-globin gene deletions.
    Fallah MS, Mahdian R, Aleyasin SA, Jamali S, Hayat-Nosaeid M, Karimipour M, Raeisi M, Zeinali S.
    Blood Cells Mol Dis; 2010 Jun 15; 45(1):58-64. PubMed ID: 20363165
    [Abstract] [Full Text] [Related]

  • 18. Molecular basis of deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia in Indian patients.
    Bhattacharya G, Banerjee D, Chandra S, Ghosh M, Chaudhuri U, Das M, Dasgupta UB.
    Clin Chim Acta; 2008 Jun 15; 392(1-2):69-70. PubMed ID: 18343225
    [No Abstract] [Full Text] [Related]

  • 19. Beta-globin gene haplotypes and alpha-thalassemia analysis in Babinga pygmies from Congo-Brazzaville.
    Mouélé R, Bodo JM, Mpelé DM, Feingold J, Galactéros F.
    Hum Biol; 2000 Apr 15; 72(2):379-83. PubMed ID: 10803667
    [Abstract] [Full Text] [Related]

  • 20. Prevalence of -alpha(3.7) and alpha alpha alpha(anti3.7) alleles in sickle cell trait and beta-thalassemia patients in Mexico.
    Nava MP, Ibarra B, Magaña MT, de la Luz Chávez M, Perea FJ.
    Blood Cells Mol Dis; 2006 Apr 15; 36(2):255-8. PubMed ID: 16466950
    [Abstract] [Full Text] [Related]

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