Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Reference55 articles.
1. Adams JG III, Boxer LA, Bahner RL, Forget BG, Tsistrakis GA, Steinberg MM (1979) Hemoglobin Indianapolis [B112 (G14) Arg]; an unstable β-chain variant producing the phenotype of severe β-thalassemia. J Clin Invest 63: 931–938
2. Agraphiotis A, Fessas P, Loukopoulos D (1978) Haematological, biochemical and biosynthetic differences between β∘ and β+ thalassemia heterozygotes. Proc. 17th Congress International Society of Haematology, Paris, p 435
3. Antonarakis S, Kazazian HH jr, Orkin SH (1985) DNA polymorphism and molecular pathology of the human globin gene clusters. Hum Genet 69: 1–14
4. Beris P, Miescher PA, Diaz-Chico JC, Han I-S, Kutlar A, Hu H, Wilson JB, Huisman THJ (1988) Inclusion-body β-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended β chain carboxy-terminus due to a modification in codon β114. Blood 72: 801–805
5. Clegg JB, Weatherall DJ, Milner PF (1971) Haemoglobin Constant-Spring — a chain termination mutant? Nature 234: 337–340
Cited by
7 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