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Journal Abstract Search

175 related items for PubMed ID: 18236737

  • 21. The heterogeneity of normal Hb A2-beta thalassaemia in Greece.
    Kattamis C, Metaxotou-Mavromati A, Wood WG, Nash JR, Weatherall DJ.
    Br J Haematol; 1979 May; 42(1):109-23. PubMed ID: 465353
    [Abstract] [Full Text] [Related]

  • 22. Molecular variants and clinical importance of beta-thalassaemia traits found in the state of Orissa, India.
    Nishank SS, Ranjit M, Kar SK, Chhotray GP.
    Hematology; 2009 Oct; 14(5):290-6. PubMed ID: 19843386
    [Abstract] [Full Text] [Related]

  • 23. The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies.
    Traeger-Synodinos J, Kanavakis E, Vrettou C, Maragoudaki E, Michael T, Metaxotou-Mavromati A, Kattamis C.
    Br J Haematol; 1996 Dec; 95(3):467-71. PubMed ID: 8943886
    [Abstract] [Full Text] [Related]

  • 24. 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; 34(1):57-62. PubMed ID: 22870600
    [Abstract] [Full Text] [Related]

  • 25. Variations in globin synthesis in delta-beta-thalassaemia.
    Kinney TR, Friedman S, Cifuentes E, Kim HC, Schwartz E.
    Br J Haematol; 1978 Jan; 38(1):15-22. PubMed ID: 638060
    [Abstract] [Full Text] [Related]

  • 26. Haemoglobin D Punjab. Interaction with alpha thalassaemia and diagnosis by gene mapping.
    Trent RJ, Harris MG, Fleming PJ, Wyatt K, Hughes WG, Kronenberg H.
    Scand J Haematol; 1984 Mar; 32(3):275-82. PubMed ID: 6322284
    [Abstract] [Full Text] [Related]

  • 27. Screening and genetic diagnosis of haemoglobin disorders.
    Old JM.
    Blood Rev; 2003 Mar; 17(1):43-53. PubMed ID: 12490210
    [Abstract] [Full Text] [Related]

  • 28. Haematological and genetic features of deltabeta-thalassaemia in Pakistan.
    Ahmed S, Anwar M.
    J Coll Physicians Surg Pak; 2006 Jan; 16(1):19-22. PubMed ID: 16441982
    [Abstract] [Full Text] [Related]

  • 29. Hb Arta [beta 45 (CD4) Phe-->Cys]: a new unstable haemoglobin with reduced oxygen affinity in trans with beta-thalassaemia.
    Vassilopoulos G, Papassotiriou I, Voskaridou E, Stamoulakatou A, Premetis E, Kister J, Marden M, Griffon N, Poyart C, Wajcman H.
    Br J Haematol; 1995 Nov; 91(3):595-601. PubMed ID: 8555060
    [Abstract] [Full Text] [Related]

  • 30. An intriguing high performance liquid chromatogram of a double heterozygosity for Hb Q-India/Hb D-Punjab.
    Badyal RK, Chhabra S, Sharma P, Das R.
    Hemoglobin; 2014 Nov; 38(6):440-3. PubMed ID: 25354131
    [Abstract] [Full Text] [Related]

  • 31. [Analysis of the phenotype-genotype relationship of hemoglobin Q-Thailand in Guangxi].
    Li Y, Chen Z, Liang L, Li R, Liang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):164-8. PubMed ID: 27060306
    [Abstract] [Full Text] [Related]

  • 32. Alpha-thalassaemia trait in various racial groups in the United Kingdom: characterization of a variant of alpha-thalassaemia in Indians.
    Walford DM, Deacon R.
    Br J Haematol; 1976 Oct; 34(2):193-206. PubMed ID: 974033
    [Abstract] [Full Text] [Related]

  • 33. A complex haemoglobinopathy diagnosis in a family with both beta zero- and alpha (zero/+)-thalassaemia homozygosity.
    Giordano PC, Harteveld CL, Bok LA, van Delft P, Batelaan D, Beemer FA, Bernini LF.
    Eur J Hum Genet; 1999 Oct; 7(2):163-8. PubMed ID: 10196699
    [Abstract] [Full Text] [Related]

  • 34. Genetic interaction of beta-thalassaemia (Hb betaT-) & haemoglobin E (Hb betaE) in populations of Eastern India.
    Ajmani M, Sharma A, Talukder G, Bhattacharyya DK.
    Indian J Exp Biol; 1977 Jun; 15(6):455-7. PubMed ID: 598876
    [No Abstract] [Full Text] [Related]

  • 35. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
    Adeyemo T, Ojewunmi O, Oyetunji A.
    Pan Afr Med J; 2014 Jun; 18():71. PubMed ID: 25400838
    [Abstract] [Full Text] [Related]

  • 36. Diagnosis of a rare double heterozygous Hb D Punjab/Hb Q India hemoglobinopathy using Sebia capillary zone electrophoresis.
    Parab S, Sakhare S, Sengupta C, Velumani A.
    Indian J Pathol Microbiol; 2014 Jun; 57(4):626-8. PubMed ID: 25308024
    [Abstract] [Full Text] [Related]

  • 37. 'Silent' beta-thalassaemia caused by a 'silent' beta-chain mutant: the pathogenesis of a syndrome of thalassaemia intermedia.
    Fessas P, Loukopoulos D, Loutradi-Anagnostou A, Komis G.
    Br J Haematol; 1982 Aug; 51(4):577-83. PubMed ID: 7104238
    [Abstract] [Full Text] [Related]

  • 38. Haemoglobin D-beta-thalassaemia in a German family. A double heterozygous haemoglobinopathy.
    Piechowiak H, Krause M, Kohne E.
    Klin Wochenschr; 1985 Jul 01; 63(13):613-5. PubMed ID: 4032984
    [Abstract] [Full Text] [Related]

  • 39. Haemoglobin D and D thalassaemia. A family report, comprising 18 members.
    Tsistrakis GA, Scampardonis GJ, Clonizakis JP, Concouris LL.
    Acta Haematol; 1975 Jul 01; 54(3):172-9. PubMed ID: 809961
    [Abstract] [Full Text] [Related]

  • 40. Haemoglobin GPhiladelphia and its interaction with haemoglobin S and alpha-thalassaemia in Nigerians.
    Knox-Macaulay HH, Fleming AF, Lamb J, Mba EC.
    Clin Lab Haematol; 1984 Jul 01; 6(2):113-21. PubMed ID: 6488738
    [Abstract] [Full Text] [Related]

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