DISORDERED GLOBIN SYNTHESIS IN THALASSEMIA
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.1749-6632.1969.tb27795.x/fullpdf
Reference9 articles.
1. Excess α Chain Synthesis Relative to β Chain Synthesis in Thalassaemia Major and Minor
2. Absence of beta Globin Synthesis and Excess of alpha Globin Synthesis in Homozygous beta-Thalassemia
3. Haemoglobin Synthesis in α-Thalassaemia (Haemoglobin H Disease)
4. J. B. Clegg, D. J. Weatherall, S. Na-Nakorn, and P. Wasi, 1968 . Haemoglobin synthesis in beta-thalassaemia . NatureIn press.
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1. David John Weatherall: haematologist and geneticist whose work on thalassaemia showed the potential of molecular medicine;BMJ;2019-01-10
2. The Role of the Inherited Disorders of Hemoglobin, the First “Molecular Diseases,” in the Future of Human Genetics;Annual Review of Genomics and Human Genetics;2013-08-31
3. Microsatellite Markers within —SEA Breakpoints for Prenatal Diagnosis of HbBarts Hydrops Fetalis;Clinical Chemistry;2007-02-01
4. The Thalassemias: The Role of Molecular Genetics in an Evolving Global Health Problem**Previously presented at the annual meeting of The American Society of Human Genetics, in Los Angeles, on November 7, 2003.;The American Journal of Human Genetics;2004-03
5. Human globin gene expression: Control of β, δ and δβ chain production;Cell;1978-10
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