X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: Detection of heterozygotes by selective medium
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine,Ecology, Evolution, Behavior and Systematics,Biochemistry
Link
http://link.springer.com/content/pdf/10.1007/BF00485754.pdf
Reference12 articles.
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3. DeMars, R., Sarto, G., Felix, J. S., and Benke, P. (1969) Lesch-Nyhan mutation: Prenatal detection with amniotic fluid cells. Science 164 1303.
4. Fujimoto, W. Y., Uhlendorf, B. W., Jacobson, C. B., and Seegmiller, J. E. (1968). Biochemical diagnosis of an X-linked disease in utero. Lancet 2 511.
5. Kelley, W. N., Greene, M. L., Rosenbloom, F. M., Henderson, J. F., and Seegmiller, J. E. (1969). Hypoxanthine-guanine phosphoribosyl-transferase deficiency in gout. Ann. Internal Med. 70 155.
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