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Browsing by Author Linden, I.J. van der

Full Text	Issue Date	Title	Author(s)
	2008	Inhibition of methylation and changes in gene expression in relation to neural tube defects.	Linden, I.J. van der; Heil, S.G.; Petersen, M.; Straaten, H.W.M. van; Heijer, M. den, et al
	2007	The 894G>T variant in the endothelial nitric oxide synthase gene and spina bifida risk	Linden, I.J. van der; Heil, S.G.; Heijer, M. den; Heijer, M. den; Blom, H.J.
	2007	Variation and expression of dihydrofolate reductase (DHFR) in relation to spina bifida.	Linden, I.J. van der; Nguyen, U.; Heil, S.G.; Franke, B.; Vloet, S.T.M., et al
	2007	Molecular genetic analysis of the human dihydrofolate reductase gene: relation with plasma total homocysteine, serum and red blood cell folate levels.	Gellekink, H.; Blom, H.J.; Linden, I.J. van der; Heijer, M. den; Heijer, M. den
	2007	The methylenetetrahydrofolate dehydrogenase (MTHFD1) 1958G>A variant is not associated with spina bifida risk in the Dutch population.	Linden, I.J. van der; Heil, S.G.; Kouwenberg, I.C.; Heijer, M. den; Blom, H.J.
	2006	The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida.	Linden, I.J. van der; Heijer, M. den; Afman, L.A.; Gellekink, H.; Vermeulen, S., et al
	2006	MTRR 66A>G polymorphism in relation to congenital heart defects.	Beijnum, I.M. van; Kouwenberg, M.; Kapusta, L.; Heijer, M. den; Linden, I.J. van der, et al
	2006	Genetic variation in genes of folate metabolism and neural-tube defect risk.	Linden, I.J. van der; Afman, L.A.; Heil, S.G.; Blom, H.J.