Different molecular defects of Gγ (Aγδβ)°-thalassaemia in Thailand
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1987.tb00746.x/fullpdf
Reference18 articles.
1. Characterization of deletions which affect the expression of fetal globin genes in man;Fritsch;Nature,1979
2. Major rearrangement in the human β-globin gene cluster;Jones;Nature,1981
3. Restriction mapping of a new deletion responsible for gγ (δβ)° thalassaemia;Jones;Nuc Acids Res,1981
4. (Aγδβ)°-thalassaemia: similarity of phenotype in four different molecular defects, including one newly described;Trent;Br J Haematol,1984
5. Restriction endonuclease gene mapping studies of an Indian (Aγδβ)° -thalassaemia, previously identified as Gγ-HPFH;Nakatsuji;Br J Haematol,1984
Cited by 4 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. The Thalassemia Repository (Ninth Edition; Part II);Hemoglobin;1998-01
2. Hemoglobinopathies in Southeast Asia: Molecular Biology and Clinical Medicine;Hemoglobin;1997-01
3. Nondeletional type of hereditary persistence of fetal haemoglobin: molecular characterization of three unrelated Thai HPFH;British Journal of Haematology;1994-08
4. Thai Gγ(Aγ δβ)°-Thalassemia and its Interaction with a Single γ-GLOBIN Gene on a Chromosome Carrying β°-Thalassemia;Hemoglobin;1990-01
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