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Journal Abstract Search

88 related items for PubMed ID: 6201079

  • 1. Molecular genetics of the sickling syndromes: evolution of new strategies for improved diagnosis.
    Benz EJ.
    Am J Pediatr Hematol Oncol; 1984; 6(1):59-66. PubMed ID: 6201079
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  • 2. Rapid detection of fetal Mendelian disorders: thalassemia and sickle cell syndromes.
    Traeger-Synodinos J, Vrettou C, Kanavakis E.
    Methods Mol Biol; 2008; 444():133-45. PubMed ID: 18425477
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  • 3. Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia.
    Nagel RL, Steinberg MH.
    Pediatr Pathol Mol Med; 2001; 20(2):123-36. PubMed ID: 12673837
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  • 9. Hemoglobin switching and its clinical implications.
    Blau CA, Stamatoyannopoulos G.
    Curr Opin Hematol; 1994 Mar; 1(2):136-42. PubMed ID: 9371272
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  • 10. Thalassemia syndromes. Recent advances.
    Ohene-Frempong K, Rappaport E, Schwartz E.
    Hematol Oncol Clin North Am; 1987 Sep; 1(3):503-19. PubMed ID: 3329184
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  • 11. Sickle cell disease: a multigenic perspective of a single gene disorder.
    Kutlar A.
    Hemoglobin; 2007 Sep; 31(2):209-24. PubMed ID: 17486504
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  • 15. Beta-S gene cluster haplotypes modulate hematologic and hemorheologic expression in sickle cell anemia. Use in predicting clinical severity.
    Powars DR, Meiselman HJ, Fisher TC, Hiti A, Johnson C.
    Am J Pediatr Hematol Oncol; 1994 Feb; 16(1):55-61. PubMed ID: 7508688
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  • 16. Polymorphism and molecular pathology of the human beta-globin gene.
    Orkin SH, Antonarakis SE, Kazazian HH.
    Prog Hematol; 1983 Feb; 13():49-73. PubMed ID: 6366914
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  • 17. Silent thalassemias: genotypes and phenotypes.
    Bianco I, Cappabianca MP, Foglietta E, Lerone M, Deidda G, Morlupi L, Grisanti P, Ponzini D, Rinaldi S, Graziani B.
    Haematologica; 1997 Feb; 82(3):269-80. PubMed ID: 9234571
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  • 18. Pharmacologic induction of fetal hemoglobin synthesis: cellular and molecular mechanisms.
    Yang YM, Pace B.
    Pediatr Pathol Mol Med; 2001 Feb; 20(1):87-106. PubMed ID: 12673846
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  • 19. Prenatal diagnosis by DNA analysis.
    Kan YW, Chang JC, Dozy AM.
    Birth Defects Orig Artic Ser; 1982 Feb; 18(7):275-83. PubMed ID: 6297633
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  • 20. Recent advances in globin gene transfer for the treatment of beta-thalassemia and sickle cell anemia.
    Sadelain M.
    Curr Opin Hematol; 2006 May; 13(3):142-8. PubMed ID: 16567956
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