Relationship of Hemoglobin Bart's and H To Alpha Thalassemia*
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.1965.tb54047.x/fullpdf
Reference12 articles.
1. Observations on some “fast” hemoglobins: K, J, N and “Bart's.” Brit;AGAR;Med. J.,1958
2. Description d'une nouvelle variete d'anemie hemolytique congenitale: etude hematologique, electrophoretique et genetique;GOUTTAS;Sang,1955
3. Studies on the hemoglobins of newborn Nigerians;HENDRICKSE;Brit. Med. J.,1960
4. Hemoglobin Bart's: A fetal hemoglobin without α-chains;HUNT;Nature,1959
5. Alpha-chain thalassemia and hydrops fetalis in Malaya: Report of five cases;LIE-INJO;Blood,1962
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1. EF Bart’s Disease with Coinheritance of Gγ-XmnI and Aγ-Globin Polymorphisms: A Case of Nontransfusion-Dependant Thalassemia;Case Reports in Hematology;2020-10-30
2. Thalassemia: a look to the future;Annals of the New York Academy of Sciences;2016-02-11
3. Haemoglobin D Punjab Interaction with α thalassaemia and diagnosis by gene mapping;Scandinavian Journal of Haematology;2009-04-24
4. Phenotypic Variation in Sickle Cell Trait;Scandinavian Journal of Haematology;2009-04-24
5. Assembly of normal and abnormal human hemoglobins;Trends in Biochemical Sciences;1981-01
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