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Journal Abstract Search

132 related items for PubMed ID: 8250015

  • 1. Quantities of alpha Q chain variants in heterozygotes with and without a concomitant beta-thalassemia trait.
    Qin WB, Baysal E, Wong KF, Molchanova TP, Pobedimskaya DD, Sharma S, Wilson JB, Huisman TH.
    Am J Hematol; 1994 Jan; 45(1):91-3. PubMed ID: 8250015
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  • 3. Hb Lulu Island (alpha 2 beta 2 107[G9]Gly-->Asp)-beta zero- thalassemia (codon 15; TGG-->TAG), a form of thalassemia intermedia.
    Gray GR, Manson HE, Gu LH, Leonova JYe, Huisman TH.
    Am J Hematol; 1995 Sep; 50(1):26-9. PubMed ID: 7668221
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  • 5. Prenatal diagnosis of beta-thalassemia major by high-performance liquid chromatography analysis of hemoglobins in fetal blood samples.
    Sanguansermsri T, Thanarattanakorn P, Steger HF, Tongsong T, Chanprapaph P, Wanpirak C, Siriwatanapa P, Sirichotiyakul S, Flatz G.
    Hemoglobin; 2001 Feb; 25(1):19-27. PubMed ID: 11300346
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  • 7. Missing Hb Q-India Peak in a Triple-Heterozygous Patient with Hb D-Punjab/Hb Q-India/β-Thalassemia Trait.
    Sharma P, Jandial A, Rajasekaran S, Das R, Chhabra S, Hira JK, Khadwal AR, Malhotra P, Sharma P.
    Hemoglobin; 2020 May; 44(3):211-213. PubMed ID: 32448026
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  • 8. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J, Papassotiriou I, Metaxotou-Mavrommati A, Vrettou C, Stamoulakatou A, Kanavakis E.
    Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
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  • 13. Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.
    Divoky V, Bissé E, Wilson JB, Gu LH, Wieland H, Heinrichs I, Prior JF, Huisman TH.
    Biochim Biophys Acta; 1992 Dec 10; 1180(2):173-9. PubMed ID: 1463768
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  • 16. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene.
    Panyasai S, Jaiping K, Pornprasert S.
    Hemoglobin; 2015 Dec 10; 39(4):292-5. PubMed ID: 26029792
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  • 19. 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 10; 40(2):75-84. PubMed ID: 26635043
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