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Journal Abstract Search

209 related items for PubMed ID: 26154945

  • 21. Analysis of deletional hereditary persistence of fetal hemoglobin/δβ-thalassemia and δ-globin gene mutations in Southerwestern China.
    Zhang J, Yang Y, Li P, Yan Y, Lv T, Zhao T, Zeng X, Li D, Zhou X, Chen H, Su J, Yang T, He J, Zhu B.
    Mol Genet Genomic Med; 2019 Jun; 7(6):e706. PubMed ID: 31044540
    [Abstract] [Full Text] [Related]

  • 22. Development of a rapid multiplex PCR assay for identification of the three common Hemoglobin-Lepore variants (Boston-Washington, Baltimore, and Hollandia) and identification of a new Lepore variant.
    Nussenzveig RH, Vanhille DL, Hussey D, Reading NS, Agarwal AM.
    Am J Hematol; 2012 Oct; 87(10):E74-5. PubMed ID: 23001912
    [No Abstract] [Full Text] [Related]

  • 23. Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ)0-Thalassemia among Tunisian family.
    Kalai M, Moumni I, Ouragini H, Ben Fraj I, Mellouli F, Ouederni M, Chaouachi D, Boudriga I, Menif S.
    Ann Clin Biochem; 2023 Mar; 60(2):81-85. PubMed ID: 36214153
    [Abstract] [Full Text] [Related]

  • 24. 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
    [Abstract] [Full Text] [Related]

  • 25. Known and new δ-globin gene mutations and other factors influencing Hb A2 measurement in the Omani population.
    Hassan SM, Harteveld CL, Bakker E, Giordano PC.
    Hemoglobin; 2014 Jun; 38(4):299-302. PubMed ID: 24985928
    [Abstract] [Full Text] [Related]

  • 26. 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 Jun; 32(5):498-504. PubMed ID: 18932076
    [Abstract] [Full Text] [Related]

  • 27. 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 Jun; 31(4):463-9. PubMed ID: 17994380
    [Abstract] [Full Text] [Related]

  • 28. IVS-II-648/649 (-T) (HBB: c.316-202del) Triggers a Novel β-Thalassemia Phenotype.
    Azimi A, Alibakhshi R, Hayati H, Tahmasebi S, Alimoradi S.
    Hemoglobin; 2017 Jan; 41(1):44-46. PubMed ID: 28475449
    [Abstract] [Full Text] [Related]

  • 29. New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG].
    Phylipsen M, Harteveld CL, de Metz M, Gallivan MV, Arkesteijn SG, Luo HY, Chui DH, Giordano PC.
    Hemoglobin; 2010 Jan; 34(5):445-50. PubMed ID: 20854118
    [Abstract] [Full Text] [Related]

  • 30. 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 Jan; 35(4):316-22. PubMed ID: 21797698
    [Abstract] [Full Text] [Related]

  • 31. Detection of a novel βδ-globin fusion gene, anti-lepore Hb CHORI (β(through IVS-I-57)/δ(from IVS-I-101)), by multiplex ligation-dependent probe amplification.
    Cui J, Azimi M, Hoppe CC.
    Hemoglobin; 2014 Jan; 38(1):60-3. PubMed ID: 24102354
    [Abstract] [Full Text] [Related]

  • 32. 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 Jan; 34(4):343-53. PubMed ID: 20642332
    [Abstract] [Full Text] [Related]

  • 33. Contrasting co-inheritance of alpha and beta mutations in delta beta thalassemia and hereditary persistence of fetal hemoglobin: a study from India.
    Pandey H, Ranjan R, Singh K, Sharma A, Kishor K, Seth T, Saxena R.
    Hematology; 2018 Oct; 23(9):692-696. PubMed ID: 29621931
    [Abstract] [Full Text] [Related]

  • 34. [Delta⁰-thalassemia by insertion of 27 base pairs in δ-globin gene with decreased hemoglobin A₂ levels].
    González Borrachero ML, de la Fuente-Gonzalo F, González FA, Nieto JM, Villegas A, Ropero P.
    Med Clin (Barc); 2015 Apr 08; 144(7):312-6. PubMed ID: 25579773
    [Abstract] [Full Text] [Related]

  • 35. First Report of a Novel Deletion Due to εγδβ-Thalassemia in a Chinese Family.
    Hui ASY, Au PKC, Ting YH, Kan ASY, Cheng YKY, Leung AWK, Chan KYK, Li CK, Tang MHY, Leung TY.
    Hemoglobin; 2017 May 08; 41(3):175-179. PubMed ID: 28950778
    [Abstract] [Full Text] [Related]

  • 36. Association of an α-globin gene cluster duplication and heterozygous β-thalassemia in a patient with a severe thalassemia syndrome.
    Jiang H, Liu S, Zhang YL, Wan JH, Li R, Li DZ.
    Hemoglobin; 2015 May 08; 39(2):102-6. PubMed ID: 25690803
    [Abstract] [Full Text] [Related]

  • 37. Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation.
    Ozkinay F, Onay H, Karaca E, Arslan E, Erturk B, Ece Solmaz A, Tekin IM, Cogulu O, Aydinok Y, Vergin C.
    Hemoglobin; 2015 May 08; 39(4):230-4. PubMed ID: 26076395
    [Abstract] [Full Text] [Related]

  • 38. Genotypic-phenotypic heterogeneity of δβ-thalassemia and hereditary persistence of fetal hemoglobin (HPFH) in India.
    Hariharan P, Kishnani P, Sawant P, Gorivale M, Mehta P, Kargutkar N, Colah R, Nadkarni A.
    Ann Hematol; 2020 Jul 08; 99(7):1475-1483. PubMed ID: 32524201
    [Abstract] [Full Text] [Related]

  • 39. Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in Cis.
    Colaco S, Trivedi A, Colah RB, Ghosh K, Nadkarni AH.
    Hemoglobin; 2014 Jul 08; 38(1):24-7. PubMed ID: 24200152
    [Abstract] [Full Text] [Related]

  • 40. The prevalence and molecular characterization of (δβ)0 -thalassemia and hereditary persistence of fetal hemoglobin in the Chinese Zhuang population.
    He S, Wei Y, Lin L, Chen Q, Yi S, Zuo Y, Wei H, Zheng C, Chen B, Qiu X.
    J Clin Lab Anal; 2018 Mar 08; 32(3):. PubMed ID: 28763119
    [Abstract] [Full Text] [Related]

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