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Journal Abstract Search

126 related items for PubMed ID: 5028129

  • 1. The clinical and biosynthetic characterization of -thalassaemia.
    Knox-Macaulay HH, Weatherall DJ, Clegg JB, Bradley J, Brown MJ.
    Br J Haematol; 1972 Apr; 22(4):497-512. PubMed ID: 5028129
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  • 3. Studies of red-cell membrane function in heterozygous beta thalassaemia and other hypochromic anaemias.
    Knox-Macaulay HH, Weatherall DJ.
    Br J Haematol; 1974 Nov; 28(3):277-97. PubMed ID: 4441462
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  • 7. The genetics of alpha-thalassemia in Yemenite and Iraqi Jews.
    Zaizov R, Kirschmann C, Matoth Y, Adam A.
    Isr J Med Sci; 1973 Nov; 9(9):1457-60. PubMed ID: 4775132
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  • 8. Absence of haemoglobin A in an individual simultaneously heterozygous in the genes for hereditary persistence of foetal haemoglobin and beta-thalassemia.
    Fogarty WM, Vedvick TS, Itano HA.
    Br J Haematol; 1974 Apr; 26(4):527-33. PubMed ID: 4846265
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  • 9. Haemoglobin H disease in a Russian family.
    Idelson LI, Didkovsky NA.
    Haematologia (Budap); 1971 Apr; 5(3):241-8. PubMed ID: 5128747
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  • 11. Haemoglobin Lepore Boston-Washington in Sicily: clinical, haematological, and biosynthetic studies.
    Schiliro G, Musumeci S, Pizzarelli G, Fischer A, Romero MA, Russo G.
    J Med Genet; 1980 Jun; 17(3):179-82. PubMed ID: 7401128
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  • 16. A case of haemoglobin J Sardegna- -thalassaemia double heterozygosis.
    Gallo E, Pugliatti L, Ricco G, Pich PG, Pinna G, Mazza U.
    Acta Haematol; 1972 Jun; 47(5):311-20. PubMed ID: 4625462
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  • 18. Molecular pathology of thalassemia syndromes.
    Marks PA, Bank A.
    Fed Proc; 1971 Jun; 30(3):977-82. PubMed ID: 5575303
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