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Journal Abstract Search

152 related items for PubMed ID: 1164567

  • 21. [Double heterozygous Hb O Arab/beta-thalassemia in a Tunisian child].
    Haji F, Chadli A, Fattoum S, Souilem J, Hassine L.
    Arch Inst Pasteur Tunis; 1985 Dec; 62(4):341-53. PubMed ID: 2423045
    [Abstract] [Full Text] [Related]

  • 22. Nature of fetal hemoglobin in the Greek type of hereditary persistence of fetal hemoglobin with and without concurrent beta-thalassemia.
    Huisman TH, Schroeder WA, Stamatoyannopoulos G, Bouver N, Shelton JR, Shelton JB, Apell G.
    J Clin Invest; 1970 May; 49(5):1035-40. PubMed ID: 5441539
    [Abstract] [Full Text] [Related]

  • 23. Regulation of the beta- and delta-hemoglobin genes. A family with hereditary persistent fetal hemoglobin and beta-thalassemia.
    Rothschild H, Bickers J, Marcus R.
    Acta Haematol; 1976 May; 56(5):285-91. PubMed ID: 826085
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  • 24. The interaction of hemoglobin E with beta thalassemia: a study of hemoglobin synthesis in a family of mixed Burmese and Iranian origin.
    Feldman R, Rieder RF.
    Blood; 1973 Nov; 42(5):783-91. PubMed ID: 4270478
    [No Abstract] [Full Text] [Related]

  • 25. [Association of alpha thalassemia and Hb G Philadelphia in a Spanish family].
    González Redondo JM, De Pablos JM.
    Sangre (Barc); 1988 Jun; 33(3):224-8. PubMed ID: 3175819
    [No Abstract] [Full Text] [Related]

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  • 27. Unusual combination of genetic defects in a Sicilian family: beta-thalassaemia, haemoglobin Lepore Boston-Washington and heterocellular hereditary persistence of fetal haemoglobin.
    Schilirò G, Musumeci S, Romeo MA, Di Gregorio F, Russo A, Testa R, Russo G.
    Br J Haematol; 1983 Nov; 55(3):473-7. PubMed ID: 6196048
    [Abstract] [Full Text] [Related]

  • 28. Hemoglobin E diseases: hematological, analytical, and biosynthetic studies in homozygotes and double heterozygotes for alpha-thalassemia.
    Wong SC, Ali MA.
    Am J Hematol; 1982 Aug; 13(1):15-21. PubMed ID: 7137163
    [Abstract] [Full Text] [Related]

  • 29. Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.
    Tan J, Tay JS, Wong YC, Kham SK, Bte Abd Aziz N, Teo SH, Wong HB.
    Southeast Asian J Trop Med Public Health; 1995 Aug; 26 Suppl 1():252-6. PubMed ID: 8629117
    [Abstract] [Full Text] [Related]

  • 30. Hb Lepore-Hb C and Hb Lepore-beta 0-thalassemia compound heterozygotes in an Algerian family.
    Francina A, Dorleac E, Aubry M, Baklouti F, Elwan S, Roda L, Phillipe N, Delaunay J.
    Hemoglobin; 1985 Aug; 9(5):505-8. PubMed ID: 4086305
    [No Abstract] [Full Text] [Related]

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  • 32. Epidemiology of Hemoglobinopathies in the Huzhou Region, Zhejiang Province, Southeast China.
    Ding ZY, Shen GS, Zhang S, He PY.
    Hemoglobin; 2016 Sep; 40(5):304-309. PubMed ID: 27615034
    [Abstract] [Full Text] [Related]

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  • 34. Hemoglobin Crete (beta 129 ala leads to pro): a new high-affinity variant interacting with beta o -and delta beta o -thalassemia.
    Maniatis A, Bousios T, Nagel RL, Balazs T, Ueda Y, Bookchin RM, Maniatis GM.
    Blood; 1979 Jul; 54(1):54-63. PubMed ID: 36184
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  • 36. Biophysical changes of red cells with thalassemia-like abnormal hemoglobin.
    Bunyaratvej A, Fucharoen S, Tatsumi N.
    Southeast Asian J Trop Med Public Health; 1992 Jul; 23 Suppl 2():86-90. PubMed ID: 1299000
    [Abstract] [Full Text] [Related]

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  • 38. Genetic heterogeneity of beta-thalassemia in southeast Sicily.
    Schilirò G, Di Gregorio F, Samperi P, Mirabile E, Liang R, Cürük MA, Ye Z, Huisman TH.
    Am J Hematol; 1995 Jan; 48(1):5-11. PubMed ID: 7530406
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  • 40. Compound heterozygotes and beta-thalassemia: top-down mass spectrometry for detection of hemoglobinopathies.
    Edwards RL, Griffiths P, Bunch J, Cooper HJ.
    Proteomics; 2014 May; 14(10):1232-8. PubMed ID: 24482221
    [Abstract] [Full Text] [Related]

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