Biochemical Phenotypes of Thalassemia in the American Negro Population*
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.tb54046.x/fullpdf
Reference8 articles.
1. The diagnosis of thalassemia trait by starch block electrophoresis of the hemoglobin;GERALD;Blood,1958
2. Reciprocal relationship of hemoglobins A2 and F in beta chain thalassemia, a key to the genetic control of hemoglobin F;ZUELZER;Blood,1961
3. Demonstration von fetalem hamoglobin in den erythrocyren eines blutausstrichs;KLEIHAUER;Klin. Wschr.,1957
4. FESSAS , P. 1964
5. Types of thalassemia-trait carriers as revealed by a study of their incidences in Greece;MALAMOS;Brit. J. Haemat.,1962
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3. Phenotypic Variation in Sickle Cell Trait;Scandinavian Journal of Haematology;2009-04-24
4. Clinical, hematological and genetic features of sickle-cell anemia and sickle cell-β thalassemia in a Brazilian population;Clinical Genetics;2008-04-23
5. Hematological status of β-thalassemics in Madras;The Indian Journal of Pediatrics;1994-05
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