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Journal Abstract Search

135 related items for PubMed ID: 29737888

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

  • 2. 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; 45(6):387-391. PubMed ID: 35168445
    [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 Nov; 34(6):594-8. PubMed ID: 21077769
    [Abstract] [Full Text] [Related]

  • 4. 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; 40(3):213-4. PubMed ID: 27117573
    [Abstract] [Full Text] [Related]

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

  • 6. 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]

  • 7. Molecular and Hematological Characterization of Two Novel δ-Globin Gene Mutations Found in Chinese Individuals.
    Sun M, Lou J, Zhao Y, Liu Y.
    Hemoglobin; 2018 Mar; 42(2):132-134. PubMed ID: 29722583
    [Abstract] [Full Text] [Related]

  • 8. Co-inheritance of β- and δ-thalassemia compromising prenatal screening in a Chinese couple seeking prevention.
    Li J, Xie XM, Zhou JY, Li DZ.
    Fetal Diagn Ther; 2011 Mar; 30(1):73-6. PubMed ID: 21494010
    [Abstract] [Full Text] [Related]

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

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

  • 11. 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]

  • 12. Analysis of δ-globin gene mutations in the Chinese population.
    Liu N, Xie XM, Zhou JY, Li R, Liao C, Li DZ.
    Hemoglobin; 2013 Feb 18; 37(1):85-93. PubMed ID: 23215833
    [Abstract] [Full Text] [Related]

  • 13. 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 Feb 18; 35(2):162-5. PubMed ID: 21417575
    [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 18; 44(3):214-217. PubMed ID: 32605393
    [Abstract] [Full Text] [Related]

  • 15. A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels.
    Karakaya T, Silan F, Ozdemir O.
    Hemoglobin; 2022 Mar 18; 46(2):87-90. PubMed ID: 35930292
    [Abstract] [Full Text] [Related]

  • 16. 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 18; 79(5):422-8. PubMed ID: 17916081
    [Abstract] [Full Text] [Related]

  • 17. Hb A1c Determination by Capillary Electrophoresis is an Efficient Method for Detecting β-Thalassemias and Hemoglobin Variants.
    Orts JA, Zúñiga Á, Bello Y, Fabregat AB, Vicente AI.
    Hemoglobin; 2016 Sep 18; 40(5):335-340. PubMed ID: 27535164
    [Abstract] [Full Text] [Related]

  • 18. Detection of a Hb A2 -Melbourne (HBD: c.130G>A) combined with β-thalassemia in a Chinese individual.
    Li Y, Huang T, Mao T, Zhang X, Liang L, Meng M.
    J Clin Lab Anal; 2020 Sep 18; 34(9):e23401. PubMed ID: 32770585
    [Abstract] [Full Text] [Related]

  • 19. Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand.
    Panyasai S, Pornprasert S.
    Hemoglobin; 2020 May 18; 44(3):179-183. PubMed ID: 32482156
    [Abstract] [Full Text] [Related]

  • 20. Hb A2-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A2-β-Thalassemia Trait.
    Chen GL, Huang LY, Zhou JY, Li DZ.
    Hemoglobin; 2017 May 18; 41(4-6):291-292. PubMed ID: 29251016
    [Abstract] [Full Text] [Related]

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