Partial mispairing and crossing-over between β0 and δ genes as the origin of the δ β0 thalassemia gene
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/BF00277642.pdf
Reference30 articles.
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2. Baglioni, C.: The fusion of two peptide chains in hemoglobin Lepore and its interpretation as a genetic deletion. Proc. Natl. Acad. Sci. U.S.A. 48, 1880–1886 (1962)
3. Benz, E. J., Swerdlow, P. S., Forget, B. C.: Absence of functional messenger RNA activity for beta globin chain synthesis in β0-thalassemia. Blood 45, 1–10 (1975)
4. Blackwell, R. Q., Huang, J. T. H., Ro, I. H.: Hemoglobin variants in Koreans: hemoglobin G (Taegu). Science 158, 1056–1057 (1967)
5. Blackwell, R. Q., Liu, C. S., Yang, H. J., Wang, C. C., Huang, J. T. H.: Hemoglobin variant common to Chinese and North American Indians: alpha-2 beta-2 (22 glu-to-ala). Science 161, 381–382 (1968)
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