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Journal Abstract Search

209 related items for PubMed ID: 6166735

  • 21. Hemoglobin A2 in iron deficient beta-thalassemia heterozygotes.
    Galanello R, Ruggeri R, Addis M, Paglietti E, Cao A.
    Hemoglobin; 1981; 5(6):613-8. PubMed ID: 7319832
    [No Abstract] [Full Text] [Related]

  • 22. Homozygous delta thalassemia in Japan.
    Ohta Y, Yasukawa M, Saito S, Fujita S, Kobayashi Y.
    Hemoglobin; 1980; 4(3-4):417-25. PubMed ID: 6158498
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  • 24. Cord blood study on beta-thalassemia and hemoglobin E.
    Pootrakul S, Muang-sup V, Fucharoen S, Wasi P.
    Am J Med Genet; 1988 Jan; 29(1):49-57. PubMed ID: 2449818
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  • 27. Haematological characteristics of the beta 0 thalassaemia trait in Sardinian children.
    Galanello R, De Virgiliis S, Addis M, Paglietti E, Ruggeri R, Cao A.
    J Clin Pathol; 1980 Oct; 33(10):946-8. PubMed ID: 7430359
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  • 28. Deletional beta-thalassemia with high Hb A2.
    Kendall AG, Popovich BW, Rosenblatt DS, Nishioka Y.
    Hemoglobin; 1988 Oct; 12(5-6):653-4. PubMed ID: 3209408
    [No Abstract] [Full Text] [Related]

  • 29. 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 Oct; 56(5):285-91. PubMed ID: 826085
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  • 30. The interaction of alpha-thalassemia and homozygous sickle-cell disease.
    Higgs DR, Aldridge BE, Lamb J, Clegg JB, Weatherall DJ, Hayes RJ, Grandison Y, Lowrie Y, Mason KP, Serjeant BE, Serjeant GR.
    N Engl J Med; 1982 Jun 17; 306(24):1441-6. PubMed ID: 6176865
    [Abstract] [Full Text] [Related]

  • 31. The silent carrier of beta thalassemia: interaction with the typical beta thalassemic trait.
    Aicardi G, Naselli A, Sciarratta GV, Sansone G.
    Blut; 1979 Jun 18; 38(6):473-8. PubMed ID: 444685
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  • 32. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand.
    Yamsri S, Sanchaisuriya K, Fucharoen G, Sae-Ung N, Fucharoen S.
    Blood Cells Mol Dis; 2011 Aug 15; 47(2):120-4. PubMed ID: 21664157
    [Abstract] [Full Text] [Related]

  • 33. beta+ -Thalassemia intermedia. Genetic and biochemical study of a family including 3 cases.
    Philip T, Souillet G, Philippe N, Freycon F, Bektas S, Morlé L, Trabuchet G, Godet J.
    Hum Hered; 1980 Aug 15; 30(5):324-30. PubMed ID: 6156119
    [Abstract] [Full Text] [Related]

  • 34. Thalassaemia screening and confirmation of carriers in parents.
    Barrett AN, Saminathan R, Choolani M.
    Best Pract Res Clin Obstet Gynaecol; 2017 Feb 15; 39():27-40. PubMed ID: 27890718
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  • 36. Anemia in male adolescents in Singapore.
    Teo CG, Seet LC, Ting WC, Ong YW.
    Pathology; 1984 Apr 15; 16(2):141-5. PubMed ID: 6205355
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  • 37. Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.
    Galanello R, Perseu L, Perra C, Maccioni L, Barella S, Longinotti M, Cao A, Cazzola M.
    Br J Haematol; 2004 Dec 15; 127(5):604-6. PubMed ID: 15566365
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  • 38. The quantitation of haemoglobin A2 and haemoglobin F: a report of the techniques review group of the Thalassaemia Society of Victoria.
    Cauchi MN, Tauro G.
    Pathology; 1979 Apr 15; 11(2):175-9. PubMed ID: 460943
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  • 39. Comparative approach to the evaluation of hemoglobin A2 by two different methods: high-performance liquid chromatography and DE-52 microchromatography.
    Samperi P, Testa R, Mancuso M, Schilirò G.
    Acta Haematol; 1990 Apr 15; 83(4):179-82. PubMed ID: 2115713
    [Abstract] [Full Text] [Related]

  • 40. Haematological and clinical data in 200 cases of thalassaemia trait in eastern Spain.
    Vayá A, Carratalá A, Martinez C, Aznar J.
    Nouv Rev Fr Hematol (1978); 1983 Apr 15; 25(6):369-73. PubMed ID: 6198618
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