Restriction enzyme analysis of the β-globin gene in DNA from β°-thalassaemic subjects from Ferrara
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference20 articles.
1. Absence of beta Globin Synthesis and Excess of alpha Globin Synthesis in Homozygous beta-Thalassemia
2. Absence of β-Globin Synthesis and Excess of α-Globin Synthesis in Homozygous β-Thalassaemic Subjects from the Ferrara Region
3. An Attempt at Demonstrating the Existence of a Nonsense Mutation in beta-Thalassemia
4. Direct demonstration of β-globin mRNA in homozygous Ferrara β0-thalassaemia patients
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1. Biochemical polymorphism in man - its relation to disease*;Animal Blood Groups and Biochemical Genetics;2009-04-24
2. Delta Thalassemia: a Non-deletion Defect;European Journal of Biochemistry;2005-03-03
3. β-Thalassemia-? Selected pseudogenes;Medical Hypotheses;1982-12
4. beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0].;Proceedings of the National Academy of Sciences;1981-01-01
5. The Molecular Genetics of Thalassemia;Advances in Human Genetics 11;1981
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