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Journal Abstract Search

481 related items for PubMed ID: 18932077

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  • 22. Analysis of the Genotypes in a Chinese Population with Increased Hb A2 and Low Hematological Indices.
    Jiang F, Chen GL, Li J, Zhou JY, Liao C, Li DZ.
    Hemoglobin; 2018 May; 42(3):154-158. PubMed ID: 30277083
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  • 27. A Case Report of Compound Heterozygosity for β0/β+-Thalassemia Resulting from under Diagnosed β-Thalassemia Found in a Hb A'2 Sample.
    Intasai N, Phasit A, Panyasai S, Pornprasert S.
    Hemoglobin; 2019 Jan; 43(1):63-65. PubMed ID: 31037981
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  • 28. 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 Jan; 34(5):407-23. PubMed ID: 20854114
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  • 29. Prevalence of hemoglobin alpha-chain gene deletion in neonates in North of Iran.
    Mahdavi MR, Kowsarian M, Karami H, Mohseni A, Vahidshahi K, Roshan P, Hojjati MT, Ebrahimzadeh MA.
    Eur Rev Med Pharmacol Sci; 2010 Oct; 14(10):871-5. PubMed ID: 21222374
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  • 32. Hb Siam [alpha15(A13)Gly-->Arg (alpha1) (GGT-->CGT)] is a typical alpha chain hemoglobinopathy without an alpha-thalassemic effect.
    Turbpaiboon C, Svasti S, Sawangareetakul P, Winichagoon P, Srisomsap C, Siritanaratkul N, Fucharoen S, Wilairat P, Svasti J.
    Hemoglobin; 2002 Feb; 26(1):77-81. PubMed ID: 11939517
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  • 34. Association of mild and severely unstable alpha chain variants: the first observation of a compound heterozygote with Hb Setif [alpha94(G1)Asp-->Tyr (alpha2)] and Hb Agrinio [alpha29(B10)Leu-->Pro (alpha2)] in a Greek family.
    Douna V, Papassotiriou I, Stamoulakatou A, Metaxotou-Mavrommati A, Kanavakis E, Traeger-Synodinos J.
    Hemoglobin; 2008 Feb; 32(6):592-5. PubMed ID: 19065338
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  • 37. Double heterozygosity for Hb New York [beta 113 GTG-->GAG; VAL-->GLU] and beta degrees-thalassemia mutations manifests as a thalassemia trait.
    Lee AC, Ma ES, Chan AY, Szeto SC, Chan LC.
    Pediatr Hematol Oncol; 2008 Feb; 25(3):227-31. PubMed ID: 18432506
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  • 38. A novel beta-Thalassemic allele due to a two nucleotide deletion: beta76 (-GC).
    Foulon K, Rochette J, Cadet E.
    Hemoglobin; 2007 Feb; 31(1):31-7. PubMed ID: 17365003
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