Thalassaemia intermedia in a family with beta 0-thalassaemia and Hb Hasharon.

Author:

Zago M A,Costa F F,Bottura C

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference17 articles.

1. nd ed. Oxford: Blackwell Scientific Publications, 1972.

2. A study of thirty-one families with simple heterozygotes and combinations of F-thalassemia with A2-thalassemia;F.-thalassemia;Am J Med; Genetic patterns in thalassemia intermedia (constitutional microcytic anemia). Familial, hematologic and biosynthetic studies,1969

3. Different types of betathalassemia intermedia. A genetic study in 20 patients;Aksoy, M.; Dingol, G.; Erdem, S.;Acta Haematol (Basel),1978

4. 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

5. The heterogeneity of normal HbA23 thalassaemia in Greece;Kattamis, C.; Metaxou-Mavromati, A.; Wood, W.G.; Nash, JR, Weatherall; D.J.;Br J Haematol,1979

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