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	1.	Recurrent leg ulcers in a young man with hyperhomocysteinemia, factor V Leiden and impaired fibrinolysis. [electronic resource] by Kolbach, D N Veraart, J C J M Hamulyák, K Spaapen, L J M Neumann, H A M Producer: 20021120 In: Acta dermato-venereologica vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	N-acetyl-glutamate synthetase deficiency or porto-systemic shunt associated encephalopathy? [electronic resource] by Dammers, R Rubio-Gozalbo, M E Robben, S G F Bakker, J A Spaapen, L J M Forget, P Ph Producer: 20030116 In: Acta paediatrica (Oslo, Norway : 1992) vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutations in the urocanase gene UROC1 are associated with urocanic aciduria. [electronic resource] by Espinós, C Pineda, M Martínez-Rubio, D Lupo, V Ormazabal, A Vilaseca, M A Spaapen, L J M Palau, F Artuch, R Producer: 20090804 In: Journal of medical genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical and biochemical presentation of siblings with COG-7 deficiency, a lethal multiple O- and N-glycosylation disorder. [electronic resource] by Spaapen, L J M Bakker, J A van der Meer, S B Sijstermans, H J Steet, R A Wevers, R A Jaeken, J Producer: 20060130 In: Journal of inherited metabolic disease vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Expanding the clinical spectrum of 3-phosphoglycerate dehydrogenase deficiency. [electronic resource] by Tabatabaie, L Klomp, L W J Rubio-Gozalbo, M E Spaapen, L J M Haagen, A A M Dorland, L de Koning, T J Producer: 20110512 In: Journal of inherited metabolic disease vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Novel EBP gene mutations in Conradi-Hünermann-Happle syndrome. [electronic resource] by Steijlen, P M van Geel, M Vreeburg, M Marcus-Soekarman, D Spaapen, L J M Castelijns, F C M Willemsen, M van Steensel, M A M Producer: 20080410 In: The British journal of dermatology vol. 157 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)