Subject
Genetics(clinical),Genetics
Reference13 articles.
1. Besley, G. T. N., Cohen, P. T. W., Faed, M. J. W. and Wolstenholme, J. Amylo-1,6-glucosidase activity in cultured cells: A deficiency in type III glycogenosis with prenatal studies.Prenatal Diagnosis 3 (1983) 13–19
2. De Barsy, Th. and Lederer, B. Type VI glycogenosis: identification of subgroups. In Burman, D., Holton, J. B. and Pennock, C. A. (eds.).Inherited Disorders of Carbohydrate Metabolism. MTP Press, Lancaster, 1980, pp. 369–380
3. Galjaard, H.Genetic Metabolic Disease. Early Diagnosis and Prenatal Analysis. Elsevier/North Holland, Amsterdam, 1980, p. 793
4. Goji, K., Morishita, Y., Kodama, S., Takahashi, T. and Matsuo, T. Lymphocyte phosphorylase kinase activities in the sex-linked form of liver phosphorylase kinase deficiency.Eur. J. Pediatr. 143 (1985) 179–182
5. Gomori, G. A modification of the colorimetric phosphorus determination for use with the photoelectric colorimeter.J. Lab. Clin. Med. 27 (1942) 955–960
Cited by
17 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