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Journal Abstract Search

203 related items for PubMed ID: 2995233

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  • 7. Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicine.
    Akerman BR, Fujiwara TM, Lancaster GA, Morgan K, Scriver CR.
    Am J Med Genet; 1990 May; 36(1):76-84. PubMed ID: 2333910
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  • 8. Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat.
    Nicholls RD, Higgs DR, Clegg JB, Weatherall DJ.
    Blood; 1985 Jun; 65(6):1434-8. PubMed ID: 2986746
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  • 9. Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.
    Pressley L, Higgs DR, Clegg JB, Weatherall DJ.
    Proc Natl Acad Sci U S A; 1980 Jun; 77(6):3586-9. PubMed ID: 6158051
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  • 10. 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 Jun; 69(4):375-7. PubMed ID: 2580774
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  • 12. Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2.
    Galanello R, Melis MA, Maccioni L, Pirastu M, Cao A.
    Pediatr Res; 1984 Feb; 18(2):158-62. PubMed ID: 6322098
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  • 18. Dysfunctional alpha-globin genes in hemoglobin H disease in blacks: variation in restriction fragment size permits the detection of the -alpha/-alpha T genotype.
    Safaya S, Mullaney P, Rieder RF.
    Am J Hematol; 1987 Dec; 26(4):329-39. PubMed ID: 2891296
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  • 19. Characterization of a new alpha zero thalassaemia defect in the South African population.
    Vandenplas S, Higgs DR, Nicholls RD, Bester AJ, Mathew CG.
    Br J Haematol; 1987 Aug; 66(4):539-42. PubMed ID: 3663510
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