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PUBMED FOR HANDHELDS

Journal Abstract Search


413 related items for PubMed ID: 25370867

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  • 3. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM.
    Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043
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  • 6. Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia.
    Farashi S, Bayat N, Faramarzi Garous N, Ashki M, Montajabi Niat M, Vakili S, Imanian H, Zeinali S, Najmabadi H, Azarkeivan A.
    Hemoglobin; 2015; 39(3):201-6. PubMed ID: 26084319
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  • 7. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene.
    Panyasai S, Jaiping K, Pornprasert S.
    Hemoglobin; 2015; 39(4):292-5. PubMed ID: 26029792
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  • 8. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
    Moassas F, Nweder MS, Murad H.
    BMC Pediatr; 2019 Feb 18; 19(1):61. PubMed ID: 30777047
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  • 9. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.
    Prakobkaew N, Fucharoen S, Fuchareon G, Siriratmanawong N.
    Eur J Haematol; 2014 Jan 18; 92(1):73-9. PubMed ID: 24112054
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  • 10. Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran.
    Miri-Moghaddam E, Bahrami S, Naderi M, Bazi A, Karimipoor M.
    Hemoglobin; 2016 Jun 18; 40(3):173-8. PubMed ID: 27117567
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  • 12. Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A2 Levels.
    Satthakarn S, Panyasai S, Pornprasert S.
    Hemoglobin; 2020 Sep 18; 44(5):349-353. PubMed ID: 33023363
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  • 13. Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.
    Verma IC, Kleanthous M, Saxena R, Fucharoen S, Winichagoon P, Raizuddin S, Khan SN, Akbari MT, Izadyar M, Kotea N, Old JM, Ioannou PA, Khan B.
    Hemoglobin; 2007 Sep 18; 31(4):439-52. PubMed ID: 17994378
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  • 14. A large cohort of β(+)-thalassemia in Thailand: molecular, hematological and diagnostic considerations.
    Yamsri S, Singha K, Prajantasen T, Taweenan W, Fucharoen G, Sanchaisuriya K, Fucharoen S.
    Blood Cells Mol Dis; 2015 Feb 18; 54(2):164-9. PubMed ID: 25471338
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  • 16. A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (HBB: c.27delG) in a Bangladeshi Family Acquired De Novo.
    Hasan KN, Sufian A, Mazumder AK, Khaleque MA, Rahman M, Akhteruzzaman S.
    Hemoglobin; 2019 May 18; 43(3):162-165. PubMed ID: 31339392
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  • 17. Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy.
    Siriratmanawong N, Chansri W, Singsanan S, Fucharoen G, Fucharoen S.
    Hemoglobin; 2009 May 18; 33(6):507-14. PubMed ID: 19958198
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  • 18. Molecular Epidemiology of Hemoglobinopathies in Cambodia.
    Munkongdee T, Tanakulmas J, Butthep P, Winichagoon P, Main B, Yiannakis M, George J, Devenish R, Fucharoen S, Svasti S.
    Hemoglobin; 2016 Jun 18; 40(3):163-7. PubMed ID: 27117566
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