Restriction endonuclease maps of the β-like globin gene cluster in the British and Greek forms of HPFH, and for one example ofGγβ+HPFH
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1982.tb01936.x/fullpdf
Reference25 articles.
1. The primary structure of the human ε-globin gene
2. Physical mapping of the globin gene deletion in hereditary persistence of foetal haemoglobin (HPFH)
3. Physical mapping of the globin gene deletion in (δβ)° - thalassaemia
4. Occurrence ofGγ Hb F in Greek HPFH: Analysis of Heterozygotes and Compound Heterozygotes with β Thalassaemia
5. Globin chain synthesis in single erythroid bursts from cord blood: studies on gamma leads to beta and G gamma leads to A gamma switches.
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1. Regulated expression of cloned human fetal Agamma-globin genes introduced into murine erythroleukemia cells;European Journal of Biochemistry;1986-09
2. The Ratio of theG? andA? Chains: Variations due to Anomalies at the Molecular Level;Annals of the New York Academy of Sciences;1985-06
3. Molecular Analysis of Deletion and Nondeletion Hereditary Persistence of Fetal Hemoglobin and Identification of a New Mutation Causing ?-Thalassemia;Annals of the New York Academy of Sciences;1985-06
4. The sequence of theAγ globin gene in aGγβ+type of hereditary persistence of fetal haemoglobin;British Journal of Haematology;1985-02
5. A point mutation in the Aγ-globin gene promoter in Greek hereditary persistence of fetal haemoglobin;Nature;1985-01
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