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Journal Abstract Search

118 related items for PubMed ID: 3209408

  • 1. Deletional beta-thalassemia with high Hb A2.
    Kendall AG, Popovich BW, Rosenblatt DS, Nishioka Y.
    Hemoglobin; 1988; 12(5-6):653-4. PubMed ID: 3209408
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  • 3. Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levels.
    Galanello R, Melis MA, Furbetta M, Angius A, Scalas MT, Paglietti E, Cao A.
    Nouv Rev Fr Hematol (1978); 1981; 23(4):193-5. PubMed ID: 7312613
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  • 4. Characterization of a new alpha-thalassemia-1 deletion in a Spanish family.
    Gonzalez-Redondo JM, Gilsanz F, Ricard P.
    Hemoglobin; 1989; 13(2):103-16. PubMed ID: 2544542
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  • 5. Australian beta zero-thalassaemia: a high haemoglobin A2 beta zero-thalassaemia due to a 12 kb deletion commencing 5' to the beta-globin gene.
    Motum PI, Lindeman R, Hamilton TJ, Trent RJ.
    Br J Haematol; 1992 Sep; 82(1):107-13. PubMed ID: 1419783
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  • 8. 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; 127(5):604-6. PubMed ID: 15566365
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  • 9. [Experience with a simple microchromatographic method for hemoglobin A2 quantification (Hb a2)].
    de Pablos Gallego JM, Cano Trapero R.
    Sangre (Barc); 1984 Dec; 29(3):314-20. PubMed ID: 6484780
    [No Abstract] [Full Text] [Related]

  • 10. Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia.
    Kalamaras A, Chassanidis C, Samara M, Papadakis MN, Vagena A, Aleporou-Marinou V, Patrinos GP, Kollia P.
    Am J Hematol; 2008 Sep; 83(9):760. PubMed ID: 18615450
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  • 11. Prospective study of red blood cell indices, hemoglobin A2, and hemoglobin F in infants heterozygous for Beta-thalassemia.
    Galanello R, Melis MA, Ruggeri R, Cao A.
    J Pediatr; 1981 Jul; 99(1):105-8. PubMed ID: 6166735
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  • 13. Hematologic changes and hemoglobin analysis beta thalassemia heterozygotes during the first year of life.
    Wood WG, Weatherall DJ, Hart GH, Bennett M, Marsh GW.
    Pediatr Res; 1982 Apr; 16(4 Pt 1):286-9. PubMed ID: 6176934
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  • 14. [Changes in hemoglobin fractions of pregnant women with heterozygous beta-thalassemia and iron deficiency anemia].
    Tikhonova LV.
    Akush Ginekol (Mosk); 1983 Dec; (12):41-3. PubMed ID: 6198936
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  • 15. A greater than 200 kb deletion removing the entire beta-like globin gene cluster in a family of Irish descent.
    Fortina P, Delgrosso K, Werner E, Haines K, Rappaport E, Schwartz E, Surrey S.
    Hemoglobin; 1991 Dec; 15(1-2):23-41. PubMed ID: 1717405
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  • 18. Alpha zero- and beta zero-thalassemia in a Thai family: unusually mild homozygous beta zero-thalassemia without alpha-globin gene deletion.
    Yenchitsomanus P, Summers KM.
    Hum Genet; 1985 Dec; 69(4):375-7. PubMed ID: 2580774
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  • 19. [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
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  • 20. 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
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