Interaction of  - and   0-thalassaemia: haematological features and globin chain synthesis analysis

Author:

Galanello R,Furbetta M,Melis M A,Rosatelli C,Cao A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. The thalassaemia syndromes;Weatherall, D.J.; Clegg, J.B.,1972

2. b5-thalassaemia in a Chinese family;Mann, JR, MacNeish; AS, Bannister; D, Clegg; JB, Wood; WG, Weatherall; D.J.;Br JHaematol,1972

3. A homozygote for Hb G-y type of foetal haemoglobin in India: a study of two Indian and four Negro families;Sukumaran, P.K.; Huisman, T.H.J.; Schroeder, W.A.;Br JHaematol,1972

4. A Gy type of hereditary persistence of fetal hemoglobin with,-chain production in cis;Huisman, T.H.J.; Miller, A.; Schroeder, W.A.;Am J Hum Genet,1975

5. The molecular heterogeneity of some types of hereditary persistence of fetal hemoglobin (HPFH);Huisman, T.H.J.; Miller, A.; Cook, L.; Gordon, S.; Schroeder, W.A.,1975

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Delta beta (F)-thalassaemia in Sardinia.;Journal of Medical Genetics;1982-06-01

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