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Browsing by Author Ruijter, G.J.
Showing results 1 to 5 of 5
| Full Text | Issue Date | Title | Author(s) | | 2010 | Mucopolysaccharidosis type IIID: 12 new patients and 15 novel mutations. | Valstar, M.J.; Bertoli-Avella, A.M.; Wessels, M.W.; Ruijter, G.J.; Graaf, B. de, et al |
| 2010 | Mucopolysaccharidosis type IIIA: clinical spectrum and genotype-phenotype correlations. | Valstar, M.J.; Neijs, S.; Bruggenwirth, H.T.; Olmer, R.; Ruijter, G.J., et al |
| 2008 | Clinical and genetic spectrum of Sanfilippo type C (MPS IIIC) disease in The Netherlands. | Ruijter, G.J.; Valstar, M.J.; Kamp, JM van de; Helm, RM van der; Durand, S., et al |
| 2007 | Congenital disorder of glycosylation type Ia presenting with hydrops fetalis. | Kamp, J.M. van de; Lefeber, D.J.; Ruijter, G.J.; Steggerda, S.J.; Hollander, N.S., et al |
| 2005 | External quality assurance programme for enzymatic analysis of lysosomal storage diseases: A pilot study. | Ruijter, G.J.; Boer, M. de; Weykamp, C.W.; Vries, R. de; Berg, I. den, et al |
Showing results 1 to 5 of 5
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