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Journal Abstract Search

209 related items for PubMed ID: 26154945

  • 1.
    ; . PubMed ID:
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  • 2. 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; 92(1):73-9. PubMed ID: 24112054
    [Abstract] [Full Text] [Related]

  • 3. A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization.
    Singha K, Fucharoen G, Hama A, Fucharoen S.
    Clin Biochem; 2015 Jul; 48(10-11):703-8. PubMed ID: 25866400
    [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. First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.
    Amirian A, Karimipoor M, Jafarinejad M, Taghavi M, Kordafshari A, Fathi Azar S, Mohammadi MS, Zeinali S.
    Arch Iran Med; 2011 Jan; 14(1):8-11. PubMed ID: 21194254
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  • 6. Identification of a novel δ-globin gene mutation in an Iranian family.
    Amirian A, Jafarinejad M, Kordafshari AR, Mosayyebzadeh M, Karimipoor M, Zeinali S.
    Hemoglobin; 2010 Jan; 34(6):594-8. PubMed ID: 21077769
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  • 7. Application of multiplex ligation-dependent probe amplification to screen for β-globin cluster deletions: detection of two novel deletions in a multi ethnic population.
    Cui J, Azimi M, Baysdorfer C, Vichinsky EP, Hoppe CC.
    Hemoglobin; 2013 Jan; 37(3):241-56. PubMed ID: 23577918
    [Abstract] [Full Text] [Related]

  • 8. Normal Hb A2 β-thalassemia trait: frameshift mutation (HBB: c.187_251dup) in cis with the Hb A2' δ-globin gene missense mutation (HBD: c.49G>C).
    Waye JS, Eng B, Hellens L, Hohenadel BA, Nakamura LM, Walker L.
    Hemoglobin; 2013 Jan; 37(2):201-4. PubMed ID: 23398055
    [Abstract] [Full Text] [Related]

  • 9. Characterization of the 5' and 3' breakpoints of the Spanish (δβ)0-thalassemia deletion in Mexican patients.
    Guzmán LF, Perea FJ, Morales-González KR, Sánchez-López JY, de la Cruz EI, Chávez-Velasco ML, Ibarra CB.
    Hemoglobin; 2011 Jan; 35(1):80-3. PubMed ID: 21250884
    [Abstract] [Full Text] [Related]

  • 10. Delta-Beta Thalassaemia in a Pathan Family.
    Ahmad SQ, Zafar SI, Malik HS, Ahmed S.
    J Coll Physicians Surg Pak; 2017 Nov; 27(11):722-724. PubMed ID: 29132487
    [Abstract] [Full Text] [Related]

  • 11. Genotype-phenotype relationship of the δ-thalassemia and Hb A(2) variants: observation of 52 genotypes.
    Lacerra G, Scarano C, Lagona LF, Testa R, Caruso DG, Medulla E, Friscia MG, Mastrullo L, Caldora M, Prezioso R, Gaudiano C, Magnano C, Romeo MA, Musollino G, Di Noce F, Carestia C.
    Hemoglobin; 2010 Nov; 34(5):407-23. PubMed ID: 20854114
    [Abstract] [Full Text] [Related]

  • 12. Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.
    Fornari TA, Lanaro C, Albuquerque DM, Ferreira R, Costa FF.
    Exp Biol Med (Maywood); 2017 Feb; 242(3):267-274. PubMed ID: 27591578
    [Abstract] [Full Text] [Related]

  • 13. Characterization of a novel deletion causing beta-thalassemia major in an Afghan family.
    Gallienne AE, Iberson NM, Dréau HM, Jackson H, Bignell PA, Old JM, Schuh A, Henderson SJ.
    Hemoglobin; 2010 Feb; 34(1):110-4. PubMed ID: 20113295
    [Abstract] [Full Text] [Related]

  • 14. A Woman with Missing Hb A2 Due to a Novel (εγ)δβ0-Thalassemia and a Novel δ-Globin Variant Hb A2-Gebenstorf (HBD: c.209G>A).
    Saller E, Knijnenburg J, Harteveld CL, Dutly F.
    Hemoglobin; 2020 May; 44(3):214-217. PubMed ID: 32605393
    [Abstract] [Full Text] [Related]

  • 15. Severe β-thalassemia intermedia in a compound heterozygous patient for the -30 (T>A) β(+)-thalassemia mutation and the δ(0)β(+)-Senegalese deletion.
    Griffon C, Joly P, Sénéchal A, Philit F, Francina A.
    Hemoglobin; 2010 May; 34(5):505-8. PubMed ID: 20854126
    [Abstract] [Full Text] [Related]

  • 16. Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China.
    Jiang F, Zuo L, Li D, Li J, Tang X, Chen G, Zhou J, Lu H, Liao C.
    BMC Med Genet; 2020 Feb 28; 21(1):43. PubMed ID: 32111191
    [Abstract] [Full Text] [Related]

  • 17. Molecular mechanisms underlying thalassemia intermedia in Iran.
    Neishabury M, Azarkeivan A, Oberkanins C, Esteghamat F, Amirizadeh N, Najmabadi H.
    Genet Test; 2008 Dec 28; 12(4):549-56. PubMed ID: 18939939
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  • 18. Mild Thalassemia Intermedia Due to Interaction of δβ-Thalassemia with Triplicated α-Globin Genes.
    Payán-Pernía S, Bernal Noguera S, Rojas Rodríguez E, Serra Ferrer M, Remacha Sevilla ÁF.
    Hemoglobin; 2020 Jul 28; 44(4):294-296. PubMed ID: 32693657
    [Abstract] [Full Text] [Related]

  • 19. Molecular spectrum of β-thalassemia mutations in the admixed Venezuelan population, and their linkage to β-globin gene haplotypes.
    Bravo-Urquiola M, Arends A, Gómez G, Montilla S, Gerard N, Chacin M, Berbar T, García O, García G, Velasquez D, Castillo O, Krishnamoorthy R.
    Hemoglobin; 2012 Jul 28; 36(3):209-18. PubMed ID: 22563936
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