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771 related items for PubMed ID: 17994380

  • 1. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
    Esteghamat F, Imanian H, Azarkeivan A, Pourfarzad F, Almadani N, Najmabadi H.
    Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
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  • 2. A single-tube multiplex gap-polymerase chain reaction for the detection of eight β-globin gene cluster deletions common in Southeast Asia.
    Tritipsombut J, Phylipsen M, Viprakasit V, Chalaow N, Sanchaisuriya K, Giordano PC, Fucharoen S, Harteveld CL.
    Hemoglobin; 2012; 36(6):571-80. PubMed ID: 23181748
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  • 3. Application of multiplex ligation-dependent probe amplification to screen for β-globin cluster deletions: detection of two novel deletions in a multi ethnic population.
    Cui J, Azimi M, Baysdorfer C, Vichinsky EP, Hoppe CC.
    Hemoglobin; 2013; 37(3):241-56. PubMed ID: 23577918
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  • 4. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
    Efremov GD.
    Hemoglobin; 2007; 31(1):1-15. PubMed ID: 17365000
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  • 5. Clinical and molecular characterization of β(S) and (G)γ((A)γδβ)⁰-thalassemia in eastern India.
    Patel DK, Patel M, Mashon RS, Patel S, Dash PM, Das BS.
    Hemoglobin; 2010; 34(6):604-9. PubMed ID: 21077771
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  • 6. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
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  • 10. Spectrum of beta thalassemia mutations and HbF levels in the heterozygous Moroccan population.
    Lemsaddek W, Picanço I, Seuanes F, Mahmal L, Benchekroun S, Khattab M, Nogueira P, Osório-Almeida L.
    Am J Hematol; 2003 Jul; 73(3):161-8. PubMed ID: 12827652
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  • 11. Characterization of three new deletions in the β-globin gene cluster during a screening survey in two French urban areas.
    Pissard S, Raclin V, Lacan P, Garcia C, Aguilar-Martinez P, Francina A, Joly P.
    Clin Chim Acta; 2013 Jan 16; 415():35-40. PubMed ID: 22981786
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  • 14. Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China.
    Jiang F, Zuo L, Li D, Li J, Tang X, Chen G, Zhou J, Lu H, Liao C.
    BMC Med Genet; 2020 Feb 28; 21(1):43. PubMed ID: 32111191
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  • 15. 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 28; 82(1):33-6. PubMed ID: 12574962
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  • 18. Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and deltabeta degrees thalassemia patients.
    Di Marzo R, Acuto S, Calzolari R, Maggio A.
    Exp Hematol; 2005 Nov 28; 33(11):1363-70. PubMed ID: 16263421
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  • 20. Genetic research and clinical analysis of β-globin gene cluster deletions in the Chinese population of Fujian province: A 14-year single-center experience.
    Chen M, Zhang M, Chen L, Lin N, Wang Y, Xu L, Huang H.
    J Clin Lab Anal; 2022 Feb 28; 36(2):e24181. PubMed ID: 34951062
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