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Journal Abstract Search

277 related items for PubMed ID: 20854114

  • 1. 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; 34(5):407-23. PubMed ID: 20854114
    [Abstract] [Full Text] [Related]

  • 2. 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; 38(4):299-302. PubMed ID: 24985928
    [Abstract] [Full Text] [Related]

  • 3. 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; 34(6):594-8. PubMed ID: 21077769
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
    [Abstract] [Full Text] [Related]

  • 6. HbA2-Partinico or delta(A2)Pro-->Thr, a new genetic variation in the delta-globin gene in cis to the beta(+) thal IVS-I-110 G>A, and the heterogeneity of delta-globin alleles in double heterozygotes for beta- and delta-globin gene defects.
    Lacerra G, Scarano C, Musollino G, Testa R, Prezioso R, Caruso DG, Lagona LF, Medulla E, Friscia MG, Gaudiano C, Carestia C.
    Ann Hematol; 2010 Feb; 89(2):127-34. PubMed ID: 19609526
    [Abstract] [Full Text] [Related]

  • 7. [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]

  • 8. Hb A2 Hong Kong - A novel δ-globin variant in a Chinese family masks the diagnosis of β-thalassemia trait.
    So CC, Chan AY, Luo HY, Verhovsek M, Chui DH, Ling SC, Chan LC.
    Hemoglobin; 2011 Apr 08; 35(2):162-5. PubMed ID: 21417575
    [Abstract] [Full Text] [Related]

  • 9. 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 Apr 08; 38(1):24-7. PubMed ID: 24200152
    [Abstract] [Full Text] [Related]

  • 10. 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 08; 92(1):73-9. PubMed ID: 24112054
    [Abstract] [Full Text] [Related]

  • 11. 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 08; 37(2):201-4. PubMed ID: 23398055
    [Abstract] [Full Text] [Related]

  • 12. Molecular mechanisms underlying thalassemia intermedia in Iran.
    Neishabury M, Azarkeivan A, Oberkanins C, Esteghamat F, Amirizadeh N, Najmabadi H.
    Genet Test; 2008 Dec 08; 12(4):549-56. PubMed ID: 18939939
    [Abstract] [Full Text] [Related]

  • 13. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM.
    Hemoglobin; 2016 Dec 08; 40(2):75-84. PubMed ID: 26635043
    [Abstract] [Full Text] [Related]

  • 14. A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A].
    Moumni I, Zorai A, Mahjoub S, Mosbahi I, Chaouechi D, Benromdhane N, Abbes S.
    Hemoglobin; 2014 Dec 08; 38(2):88-90. PubMed ID: 24471655
    [Abstract] [Full Text] [Related]

  • 15. 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 08; 34(1):57-62. PubMed ID: 22870600
    [Abstract] [Full Text] [Related]

  • 16. 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 Jun 08; 82(3):269-80. PubMed ID: 9234571
    [Abstract] [Full Text] [Related]

  • 17. Two new hemoglobin variants: Hb Aix-Les-Bains [β5(A2)Pro→Leu; HBB:c.17 C>T] and Hb Dubai [α122(H5)His→Leu (α2); HBA2:c.368 A>T].
    Joly P, Garcia C, Lacan P, Couprie N, Francina A.
    Hemoglobin; 2011 Jun 08; 35(2):147-51. PubMed ID: 21417572
    [Abstract] [Full Text] [Related]

  • 18. Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A2 Levels.
    Satthakarn S, Panyasai S, Pornprasert S.
    Hemoglobin; 2020 Sep 08; 44(5):349-353. PubMed ID: 33023363
    [Abstract] [Full Text] [Related]

  • 19. Delta-thalassemia in Cyprus.
    Pavlou E, Phylactides M, Kyrri A, Kalogerou E, Makariou C, Georgiou I, Kleanthous M.
    Hemoglobin; 2006 Sep 08; 30(4):455-62. PubMed ID: 16987800
    [Abstract] [Full Text] [Related]

  • 20. 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 08; 39(5):368-70. PubMed ID: 26154945
    [Abstract] [Full Text] [Related]

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