Experience with Detection of Heterozygous Carriers and Prenatal Diagnosis of Lesch-Nyhan Disease-Reference-Cited by-同舟云学术

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Experience with Detection of Heterozygous Carriers and Prenatal Diagnosis of Lesch-Nyhan Disease

Published:1977 Issue: Volume: Page:351-358
ISSN:
Container-title:Purine Metabolism in Man—II
language:
Short-container-title:

Author:

Bakay B.,Francke U.,Nyhan W. L.,Seegmiller J. E.

Publisher

Springer US

Link

http://link.springer.com/content/pdf/10.1007/978-1-4613-4223-6_44

Reference13 articles.

1. Lesch, M., and Nyhan, W.L., Am. J. Med. 36: 561 (1964).

2. Seegmiller, J.E., Rosenbloom, F.M., and Kelley, W.N., Science 155: 1682 (1967).

3. Migeon, B.R., Der Kaloustian, V.M., Nyhan, W.L., Young, W.J., and Childs, B., Science 160: 425 (1968).

4. Nyhan, W.L., Bakay, B., Connor, J.D., Marks, J.F., and Keele, D.K., Proc. Nat. Acad. Sci. USA 65: 214 (1970).

5. Albertini, R.J., and DeMars, R., Biochem. Genet. 11: 397 (1974).

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Lesch–Nyhan syndrome;Neurocutaneous Disorders;2004-01-08

2. Prenatal diagnosis of Lesch-Nyhan disease;Prenatal Diagnosis;2003

3. Inborn errors of purine metabolism;Inborn Errors of Metabolism in Humans;1982

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