-GγAγ-thalassemia and γ-chain variants in chinese newborn babies
Author:
Publisher
Wiley
Subject
Hematology
Reference22 articles.
1. The occurrence of different levels of Gγ chain and of the AγT variant of fetal hemoglobin in newborn babies from several countries;Huisman;Am J Hematol,1983
2. Gamma thalassemia resulting from the deletion of a γ-globin gene;Sukumaran;Nucleic Acids Res,1983
3. Hb F-Yamaguchi (γ75Thr, γ80Asn, γ136A1a) is associated with Gγ thalassemia;Nakatsuji;Am J Hematol,1984
4. Recent advances in the quantitation of human fetal hemoglobins with different gamma chains;Huisman;Am J Hematol,1980
Cited by 30 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. Activation of γ-globin gene expression by GATA1 and NF-Y in hereditary persistence of fetal hemoglobin;Nature Genetics;2021-08
2. The studies of hemoglobinopathies and thalassemia in China—the experiences in Shanghai Institute of Medical Genetics;Clinica Chimica Acta;2001-11
3. The association of Hb khartoum [β124(H2)Pro→Arg] with γ+-thalassemia is responsible for hemolytic disease in the newborn of a sudanese family;Hemoglobin;1999-01
4. The Thalassemia Repository (Ninth Edition; Part II);Hemoglobin;1998-01
5. International Hemoglobin Information Center Variant List;Hemoglobin;1997-01
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