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Browsing by Author Ijlst, L.
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| Full Text | Issue Date | Title | Author(s) | | 2008 | [Short-chain acyl-CoA dehydrogenase deficiency (SCADD): relatively high prevalence in the Netherlands and strongly variable fenotype; neonatal screening not indicated] | Maldegem, BT van; Duran, M.; Wanders, R.J.A.; Niezen-Koning, K.E.; Hogeveen, M., et al |
| 1997 | Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient | Huizing, M.; Iacobazzi, V.; Ijlst, L.; Savelkoul, P.J.M.; Ruitenbeek, W., et al |
Showing results 1 to 2 of 2
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