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Journal Abstract Search

401 related items for PubMed ID: 9139146

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  • 2. Compound heterozygosity of Hb D(Iran) (beta(22) Glu-->Gln) and beta(0)-thalassemia (619 bp-deletion) in India.
    Agrawal MG, Bhanushali AA, Dedhia P, Jeswani KD, Dayanand S, Dasgupta A, Das BR.
    Eur J Haematol; 2007 Sep; 79(3):248-50. PubMed ID: 17655708
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  • 3. Hemoglobin D/beta-thalassemia and beta-thalassemia major in a Saudi family.
    Owaidah TM, Al-Saleh MM, Al-Hellani AM.
    Saudi Med J; 2005 Apr; 26(4):674-7. PubMed ID: 15900384
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  • 5. Beta-thalassemia in association with a new delta-chain hemoglobin variant [delta116(g18)Arg-->Leu]: implications for carrier screening and prenatal diagnosis.
    Waye JS, Patterson M, Walker L, Eng B, Nakamura LM, Lafferty JD, Yong SL, Wu JK, Chui DH.
    Am J Hematol; 2003 Nov; 74(3):179-81. PubMed ID: 14587045
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  • 9. Hb D-Punjab [beta 121 (GH4) Glu-->Gln]/beta0-thalassemia [IVSII.1(G-->A)] in two cases from an Iranian family: first report.
    Rahimi Z, Akramipour R, Korani S, Nagel RL.
    Am J Hematol; 2006 Apr; 81(4):302-3. PubMed ID: 16550524
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  • 12. Silent thalassemias: genotypes and phenotypes.
    Bianco I, Cappabianca MP, Foglietta E, Lerone M, Deidda G, Morlupi L, Grisanti P, Ponzini D, Rinaldi S, Graziani B.
    Haematologica; 1997 Apr; 82(3):269-80. PubMed ID: 9234571
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  • 13. High incidence of the CD8/9 (+G) beta 0-thalassemia mutation in Spain.
    Villegas A, Ropero P, Ataulfo González F, Martí E, Anguita E, de Blas JM.
    Haematologica; 1998 Dec; 83(12):1066-8. PubMed ID: 9949622
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  • 18. [Hemoglobin O Arab in interaction with beta 0-thalassemia].
    Nikolov N, Andreeva M, Janković L, Efremov GD.
    Lijec Vjesn; 1989 Dec; 111(1-2):27-30. PubMed ID: 2739498
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  • 19. 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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