HEMOGLOBIN F IN ? THALASSEMIA AND RELATED CONDITIONS
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.1749-6632.1980.tb33665.x/fullpdf
Reference45 articles.
1. Evidence for multiple structural genes for the gamma chain of human fetal hemoglobin.
2. Evidence for four nonallelic structural genes for the γ chain of human fetal hemoglobin
3. Hemoglobin Kenya, the product of fusion of γ and β polypeptide chains
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1. FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999);Hemoglobin;2001-01
2. Hematological status of β-thalassemics in Madras;The Indian Journal of Pediatrics;1994-05
3. The Emerging Complexity of Genetic Control of Persistent Fetal Hemoglobin Biosynthesis in Adults;Annals of the New York Academy of Sciences;1989-07
4. An HbF enrichment procedure for the HPLC analysis of γ chains;Clinica Chimica Acta;1985-05
5. Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.;Proceedings of the National Academy of Sciences;1985-04-01
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