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Browsing by Author Spaapen, L.J.
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| Full Text | Issue Date | Title | Author(s) | | 2007 | Novel EBP gene mutations in Conradi-Hunermann-Happle syndrome. | Steijlen, P.M.; Geel, M. van; Vreeburg, M.; Marcus-Soekarman, D.; Spaapen, L.J., et al |
| 2005 | Clinical and biochemical presentation of siblings with COG-7 deficiency, a lethal multiple O- and N-glycosylation disorder. | Spaapen, L.J.; Bakker, J.A.; Meer, S.B. van der; Sijstermans, H.J.; Steet, R.A., et al |
Showing results 1 to 2 of 2
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