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Journal Abstract Search

126 related items for PubMed ID: 1201216

  • 21. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
    Adeyemo T, Ojewunmi O, Oyetunji A.
    Pan Afr Med J; 2014; 18():71. PubMed ID: 25400838
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  • 22. The Hb F composition in a Moroccan family with beta zero-thalassaemia and Hb O-Arab.
    Morlé F, Morlé L, Baklouti F, Dorléac E, Baudonnet C, Delaunay J, Godet J.
    Scand J Haematol; 1984 Sep; 33(3):281-7. PubMed ID: 6209785
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  • 23. [Clinical considerations on 7 cases of Hb C-thalassemia].
    Polosa P, Motta L, Calcagno G.
    Haematologica; 1970 Sep; 55(5):333-57. PubMed ID: 4995788
    [No Abstract] [Full Text] [Related]

  • 24. Alpha thalassaemia in Sicily: haematological and biosynthetic studies.
    Musumeci S, Schiliro G, Pizzarelli G, D'Agata A, Fischer A, Russo G.
    Br J Haematol; 1979 Nov; 43(3):413-22. PubMed ID: 497118
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  • 25. Globin biosynthesis in sickle cell, Hb SC, and Hb C diseases.
    Kim HC, Weierbach RG, Friedman S, Schwartz E.
    J Pediatr; 1977 Jul; 91(1):13-20. PubMed ID: 874650
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  • 29. The importance of the genetic picture and globin synthesis in determining the clinical and haematological features of thalassaemia intermedia.
    Gallo E, Massaro P, Miniero R, David D, Tarella C.
    Br J Haematol; 1979 Feb; 41(2):211-21. PubMed ID: 427031
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  • 36. Alpha-thalassemia does not significantly contribute to the low MCV level of Hb C trait.
    Silva NM, Soledade CS, Costa FF, Sonati MF.
    Hemoglobin; 2002 Aug; 26(3):305-9. PubMed ID: 12403496
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  • 37. Sickle cell-beta 0-thalassaemia in Saudi Arabia.
    el-Hazmi MA, Al-Swailem AR.
    Hum Hered; 1987 Aug; 37(4):211-6. PubMed ID: 2443440
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  • 38. Thalassaemia and haemoglobinopathies in Brunei Darussalam.
    Ismail JB.
    Med J Malaysia; 1992 Jun; 47(2):98-102. PubMed ID: 1494340
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