These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

173 related items for PubMed ID: 24985928

  • 1. 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]

  • 2. 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]

  • 3. 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]

  • 4. 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; 38(1):24-7. PubMed ID: 24200152
    [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. A study of δ-globin gene mutations in the UK population: identification of three novel variants and development of a novel DNA test for Hb A'2.
    Khalil MS, Marouf S, Element D, Timbs A, Gallienne A, Schuh A, Old JM, Henderson S.
    Hemoglobin; 2014 Nov; 38(3):201-6. PubMed ID: 24601842
    [Abstract] [Full Text] [Related]

  • 7. First report of the spectrum of δ-globin gene mutations in Omani subjects - identification of novel mutations.
    Alkindi S, AlZadjali S, Daar S, Ambusaidi R, Gravell D, Al Haddabi H, Krishnamoorthy R, Pathare A.
    Int J Lab Hematol; 2015 Apr; 37(2):238-43. PubMed ID: 25043855
    [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 Apr; 37(2):201-4. PubMed ID: 23398055
    [Abstract] [Full Text] [Related]

  • 9. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
    Moassas F, Nweder MS, Murad H.
    BMC Pediatr; 2019 Feb 18; 19(1):61. PubMed ID: 30777047
    [Abstract] [Full Text] [Related]

  • 10. [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]

  • 11. 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 08; 14(1):8-11. PubMed ID: 21194254
    [Abstract] [Full Text] [Related]

  • 12. Molecular Characterization of δ-Thalassemia in Iran.
    Kordafshari A, Amirian A, Zeinali S, Valaei A, Maryami F, Karimipoor M.
    Hemoglobin; 2016 Jan 08; 40(1):44-7. PubMed ID: 26754299
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. δ-Thalassemia with Complete Absence of Hb A2 in a Chinese Family.
    Tang HS, Wang DG, Huang LY, Li DZ.
    Hemoglobin; 2018 Mar 08; 42(2):135-137. PubMed ID: 29737888
    [Abstract] [Full Text] [Related]

  • 19. An Evaluation for the Causes of Reduced Hb A2 and the Molecular Characterization of HBD Variants in Hong Kong.
    Chan NCN, Wong THY, Cheng KCK, Chan NPH, Ng MHL.
    Hemoglobin; 2021 Nov 08; 45(6):387-391. PubMed ID: 35168445
    [Abstract] [Full Text] [Related]

  • 20. A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)].
    Yan JM, Zhou JY, Xie XM, Li J, Li DZ.
    Hemoglobin; 2016 Jun 08; 40(3):213-4. PubMed ID: 27117573
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.