Author:
Indrak Karel,Brabec Vaclav,Indrakova Jarmila,Chrobak Ladislav,Sakalova Adriana,Jarosova Marie,Cermak Jaroslav,Fei You-jun,Kutlar Ferdane,Gu Yuan-chao,Baysal Erol,Huisman Titus H. J.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference35 articles.
1. Bissé E, Wieland H (1988) High-performance liquid chromatographic separation of human haemoglobins: simultaneous quantitation of foetal and glycated haemoglobins. J Chromatogr 434:95–110
2. Brabec V, Borova J, Fortova H, Hrodek O, Neuwirt J, Neuvirtova R, Syristova E (1988) β-Thalassemia in Czech families. Int Med 34:979–988
3. Efremov GD, Huisman THJ (1983) The occurrence of α and β chain abnormal hemoglobins and β-thalassemia in European countries. In: Bowman JE (eds) Distribution and evolution of hemoglobin and globin loci, vol 4. Elsevier, Amsterdam, 315–344
4. Fei YJ, Kutlar F, Harris HF II, Wilson MM, Milana A, Sciacca P, Schiliro G, Masala B, Manca L, Altay C, Gurgey A, de Pablos JMa, Villegas A, Huisman THJ (1989a) A search for anomalies in the ζ, α,β, and γ globin gene arrangements in normal Black, Italian, Turkish, and Spanish newborns. Hemoglobin 13:45–65
5. Fei YJ, Stoming TA, Kutlar A, Huisman THJ, Stamatoyannopoulos G (1989b) One form of inclusion body β-thalassemia is due to a GAA→TAA mutation at codon 121 of the β chain. Blood 73:1075–1077
Cited by
40 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