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Journal Abstract Search

507 related items for PubMed ID: 25866400

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  • 3. Identification and molecular characterization of a novel 55-kb deletion recurrent in southern Italy: the Italian (G) γ((A) γδβ)°-thalassemia.
    Lacerra G, Prezioso R, Musollino G, Piluso G, Mastrullo L, De Angioletti M.
    Eur J Haematol; 2013 Mar; 90(3):214-9. PubMed ID: 23281611
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  • 5. Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH.
    Blattner A, Brunner-Agten S, Ludin K, Hergersberg M, Herklotz R, Huber AR, Röthlisberger B.
    Blood Cells Mol Dis; 2013 Jun; 51(1):39-47. PubMed ID: 23491071
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  • 8. 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 Jun; 34(6):604-9. PubMed ID: 21077771
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  • 11. 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 Jun; 33(6):507-14. PubMed ID: 19958198
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  • 12. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.
    Azma RZ, Othman A, Azman N, Alauddin H, Ithnin A, Yusof N, Razak NF, Sardi NH, Hussin NH.
    Malays J Pathol; 2012 Jun; 34(1):57-62. PubMed ID: 22870600
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  • 13. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients.
    Fucharoen S, Pengjam Y, Surapot S, Fucharoen G, Sanchaisuriya K.
    Am J Hematol; 2002 Oct; 71(2):109-13. PubMed ID: 12353310
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  • 16. Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype.
    Hariharan P, Sawant M, Gorivale M, Manchanda R, Colah R, Ghosh K, Nadkarni A.
    Mol Biol Rep; 2017 Oct; 44(5):413-417. PubMed ID: 28879539
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  • 18. Molecular mechanisms underlying thalassemia intermedia in Iran.
    Neishabury M, Azarkeivan A, Oberkanins C, Esteghamat F, Amirizadeh N, Najmabadi H.
    Genet Test; 2008 Dec; 12(4):549-56. PubMed ID: 18939939
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  • 19. [Analysis of clinical phenotype and genotype of unstable Hemoglobin Rush].
    Ge S, Yang B, Yi W, Huang K, Liu H, Huang X, Chu J, Yang Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb 10; 34(1):15-20. PubMed ID: 28186586
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