Clinical and haematological evaluation of beta thalassaemia intermedia with increased Hb F and Hb A2 in heterozygotes: beta thalassaemia intermedia I.

Author:

Altay C,Gurgey A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference22 articles.

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

2. Homozygouts beta thalassaemia in American Blacks. The problem of mild thalassaemia;Braverman, A.S.; McCurdy, P.R.; Manos, P.; Sherman, A.;J Lab Clin Med,1973

3. Kutlar A.,3-thalassaemia intermedia homozygous for normal A2,1-thalassaemia. Study in four families;Aksoy, M.; Bermek, E.; Almi§, G.;Acta Haematol,1982

4. "Silent",1-thalassaemia caused by a silent a-chain mutant: the pathogenesis of a syndrome of thalassaemia intermedia;Fessas, P.; Loukopoulos, D.; Loutradi-Anoqnostou, A.; Komis, G.;Br J Haematol,1982

5. Thalassaemia intermcdia in Cyprus. The interaction of a and fI thalassacmia;Wainscoat, J.S.; Kanavakis, E.; Wood, W.G.;Br J Haematol,1983

Cited by 3 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. Reevaluation of iron Absorption and Serum Ferritin in β-Thalassemia Intermedia;Pediatric Hematology and Oncology;1992-01

2. ?-Thalassemia Intermedia in Turkey;Annals of the New York Academy of Sciences;1990-12

3. β-Thalassemia in Turkey;Hemoglobin;1990-01

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