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Journal Abstract Search

180 related items for PubMed ID: 20113295

  • 1.
    ; . PubMed ID:
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  • 2. Molecular characterization of a beta-globin gene deletion of 1357 bp in a Taiwanese beta-thalassemia carrier.
    Huang CH, Chang YY, Chen CH, Ko TM.
    Hemoglobin; 2008; 32(5):498-504. PubMed ID: 18932076
    [Abstract] [Full Text] [Related]

  • 3. Identification of the linkage of a 1.357 KB beta-globin gene deletion and A gamma-globin gene triplication in a Chinese family.
    Lou JW, Li Q, Wei XF, Huang JW, Xu XM.
    Hemoglobin; 2010; 34(4):343-53. PubMed ID: 20642332
    [Abstract] [Full Text] [Related]

  • 4. 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.
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  • 6. Detection of unknown deletions in beta-globin gene cluster using relative quantitative PCR methods.
    Babashah S, Jamali S, Mahdian R, Nosaeid MH, Karimipoor M, Alimohammadi R, Raeisi M, Maryami F, Masoudifar M, Zeinali S.
    Eur J Haematol; 2009 Sep; 83(3):261-9. PubMed ID: 19341428
    [Abstract] [Full Text] [Related]

  • 7. A 13-bp deletion in the 3' untranslated region of the β-globin gene causes β-thalassemia major in compound heterozygosity with IVSII-1 mutation.
    Hamid M, Akbari MT.
    Med Princ Pract; 2011 Sep; 20(5):488-90. PubMed ID: 21757944
    [Abstract] [Full Text] [Related]

  • 8. Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion.
    Waye JS, Eng B, Got T, Hanna M, Hohenadel BA, Nakamura LM, Walker L.
    Hemoglobin; 2015 Sep; 39(5):368-70. PubMed ID: 26154945
    [Abstract] [Full Text] [Related]

  • 9. Multiplex ligation-dependent probe amplification screening of isolated increased HbF levels revealed three cases of novel rearrangements/deletions in the beta-globin gene cluster.
    Lee ST, Yoo EH, Kim JY, Kim JW, Ki CS.
    Br J Haematol; 2010 Jan; 148(1):154-60. PubMed ID: 19807730
    [Abstract] [Full Text] [Related]

  • 10. Molecular characterization of a Chinese pedigree with beta-thalassemia intermedia.
    Huang G, Jiang WL, Rong KB, Li YX, Luo XL, Meng JX, Yu XY.
    Hemoglobin; 2010 Jan; 34(2):179-83. PubMed ID: 20353356
    [Abstract] [Full Text] [Related]

  • 11. A family with the 619 bp deletion on the beta-globin gene found in Kerman Province, Iran.
    Saleh-Gohari N, Mashizi AK.
    Hemoglobin; 2009 Jan; 33(6):515-8. PubMed ID: 19958199
    [Abstract] [Full Text] [Related]

  • 12. A novel α(0) -thalassemia deletion in a Greek patient with HbH disease and β-thalassemia trait.
    Phylipsen M, Traeger-Synodinos J, van der Kraan M, van Delft P, Bakker G, Geerts M, Kanavakis E, Stamoulakatou A, Karagiorga M, Giordano PC, Harteveld CL.
    Eur J Haematol; 2012 Apr; 88(4):356-62. PubMed ID: 22324317
    [Abstract] [Full Text] [Related]

  • 13. Detection of a rare mutation in an Iranian family: codons 37/38/39 (7 bp deletion).
    Zadeh-Vakili A, Eshghi P.
    Hemoglobin; 2009 Apr; 33(6):523-7. PubMed ID: 19958201
    [Abstract] [Full Text] [Related]

  • 14. Comprehensive and efficient HBB mutation analysis for detection of beta-hemoglobinopathies in a pan-ethnic population.
    Chan OT, Westover KD, Dietz L, Zehnder JL, Schrijver I.
    Am J Clin Pathol; 2010 May; 133(5):700-7. PubMed ID: 20395516
    [Abstract] [Full Text] [Related]

  • 15. Dominantly Inherited beta-Thalassemia.
    Efremov GD.
    Hemoglobin; 2007 May; 31(2):193-207. PubMed ID: 17486503
    [Abstract] [Full Text] [Related]

  • 16. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
    El-Gawhary S, El-Shafie S, Niazi M, Aziz M, El-Beshlawy A.
    Hemoglobin; 2007 May; 31(1):63-9. PubMed ID: 17365006
    [Abstract] [Full Text] [Related]

  • 17. A novel deletion/insertion caused by a replication error in the β-globin gene locus control region.
    Joly P, Lacan P, Garcia C, Meley R, Pondarré C, Francina A.
    Hemoglobin; 2011 May; 35(4):316-22. PubMed ID: 21797698
    [Abstract] [Full Text] [Related]

  • 18. [Case of deletion type beta(0)-thalassemia found in an Asian (Malaysian) family living in Japan].
    Harano K, Harano T.
    Rinsho Byori; 2010 Apr; 58(4):325-31. PubMed ID: 20496759
    [Abstract] [Full Text] [Related]

  • 19. Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patients.
    Harteveld CL, Refaldi C, Cassinerio E, Cappellini MD, Giordano PC.
    Blood Cells Mol Dis; 2008 Apr; 40(3):312-6. PubMed ID: 18249014
    [Abstract] [Full Text] [Related]

  • 20. The rare codon 24 (T>A) (beta+) mutation in association with the common codon 39 (C> T) (beta0) mutation causes transfusion-dependent beta-thalassemia in a Moroccan patient.
    Agouti I, Bennani M, Levy N, Giordano P, Badens C.
    Hemoglobin; 2009 Apr; 33(2):150-4. PubMed ID: 19373592
    [Abstract] [Full Text] [Related]

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