Globin Chain Synthesis in Sicilian Thalassaemic Subjects
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1970.tb06974.x/fullpdf
Reference14 articles.
1. Observations on the Chromatographic Heterogeneity of Normal Adult and Fetal Human Hemoglobin: A Study of the Effects of Crystallization and Chromatography on the Heterogeneity and Isoleucine Content
2. Absolute Rates of Globin Chain Synthesis in Thalassemia
3. Excess α Chain Synthesis Relative to β Chain Synthesis in Thalassaemia Major and Minor
4. Absence of beta Globin Synthesis and Excess of alpha Globin Synthesis in Homozygous beta-Thalassemia
5. Excess of alpha-Globin Synthesis in Homozygous beta-Thalassemia and its Removal from the Red Blood Cell Cytoplasm
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1. Sickle cell β-thalassaemia compared with sickle cell anaemia in Algeria;Scandinavian Journal of Haematology;2009-04-24
2. β+-Thalassaemia, Haemoglobin S and Hereditary Elliptocytosis in a Zaïrian Family;Acta Haematologica;1976
3. Globin Synthesis in the Jamaican Negro with Beta-Thalassaemia;British Journal of Haematology;1974-12
4. The Molecular Basis of Thalassemi;CRC Critical Reviews in Biochemistry;1974-01
5. New mutation in a swiss girl leading to clinical and biochemical β-thalassemia minor;Humangenetik;1973-12
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