Association of heterocellular HPFH, beta(+)-thalassaemia, and delta beta(0)-thalassaemia: haematological and molecular aspects.

Author:

Cianetti L,Care A,Sposi N M,Giampaolo A,Calandrini M,Petrini M,Massa A,Marinucci M,Mavilio F,Ceccanti M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference20 articles.

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

2. Haemoglobin switching in humans;Peschle, C.; Migliaccio, G.; Migliaccio, A.R.,1983

3. Restriction endonuclease maps of the 3-globin gene cluster in the British and Greek forms of HPFH, and for one example of Gyp+HPFH;Jones, R.W.; Old, J.M.; Wood, W.G.; Clegg, J.B.; Weatherall, D.J.;Br J Haematol,1982

4. The British type of HPFH: cellular and molecular analysis of increased Hb F production;Wood, W.G.; Old, J.M.; Darbre, P.D.; Clegg, J.B.; Weatherall, D.J.; McRae, I.A.,1982

5. Cellular mechanisms of increased Hb F production in the interaction between heterocellular HPFH and P-thalassaemia;Marinucci, M.; Mavilio, F.; Gabbianelli, M.,1982

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