Bone marrow and peripheral blood globin chain synthesis in sickle cell beta zero thalassaemia.

Author:

Costa F F,Zago M A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. The clinical features of sickle cell/4-thalassemia in Jamaica;Serjeant, G.R.; Ashcroft, M.T.; Serjeant, B.; Milner, P.F.;Br J Haematol,1973

2. The thalassaemia syndromes;Weatherall, D.J.; Clegg, J.B.,1981

3. Clinical, hematological and genetic features of sickle cell-1 thalassemia in a Brazilian population;Zago, M.A.; Costa, F.F.; Freitas, T.C.; Bottura, C.;Clin Genet,1980

4. Changes in globin synthesis with erythroid cell maturation in sickle thalassemia;Bank, A.; Dow, L.W.; Farace, M.G.; O'Donnell, J.V.; Ford, S.; Natta, C.;Blood,1973

5. Globin synthesis in S/IP thalassaemia Hemoglobinopathies in children,1980

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