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Browsing by Author Berger, R.A.
Showing results 1 to 3 of 3
| Full Text | Issue Date | Title | Author(s) | | 1997 | Asymptomatic and late-onset ornithine transcarbamylase deficiency caused by a A208T mutation : Clinical, biochemical and DNA analyses in a four-generation family | Ausems, M.G.E.M.; Bakker, E.; Berger, R.A.; Duran, M.; Diggelen, O.P. van, et al |
| 1996 | Phenylketonuria in the Netherlands: 93% of the mutations are detected by single-strand conformation analysis. | Sijs-Bos, C.J.M. van der; Diepstraten, C.M.; Juyn, J.A.; Plaisier, M.; Giltay, J., et al |
| 1995 | X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase alpha subunit | Berg, I.E.T. van den; Beurden, E.A.C.M. van; Malingré, H.E.M.; Ploos van Amstel, J.K.; Poll-The, B.T., et al |
Showing results 1 to 3 of 3
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