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	1.	Prenatal diagnosis of ataxia-telangiectasia and Nijmegen Breakage syndrome by the assay of radioresistant DNA synthesis. [electronic resource] by Kleijer, W J van der Kraan, M Los, F J Jaspers, N G Producer: 19950224 In: International journal of radiation biology vol. 66 Availability: No items available. Save to lists Add to cart (remove)
	2.	Definition of an extended MHC class II-peptide binding motif for the autoimmune disease-associated Lewis rat RT1.BL molecule. [electronic resource] by Wauben, M H van der Kraan, M Grosfeld-Stulemeyer, M C Joosten, I Producer: 19970522 In: International immunology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	First-trimester prenatal diagnosis of the Nijmegen breakage syndrome and ataxia telangiectasia using an assay of radioresistant DNA synthesis. [electronic resource] by Jaspers, N G van der Kraan, M Linssen, P C Maçek, M Seemanová, E Kleijer, W J Producer: 19910228 In: Prenatal diagnosis vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Prenatal diagnosis of isovaleric acidaemia by enzyme and metabolite assay in the first and second trimesters. [electronic resource] by Kleijer, W J van der Kraan, M Huijmans, J G van den Heuvel, C M Jakobs, C Producer: 19951005 In: Prenatal diagnosis vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Two extremes of the clinical spectrum of glycogen storage disease type II in one family: a matter of genotype. [electronic resource] by Kroos, M A Van der Kraan, M Van Diggelen, O P Kleijer, W J Reuser, A J Producer: 19970319 In: Human mutation vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Atypical clinical presentation of ataxia telangiectasia. [electronic resource] by Willems, P J Van Roy, B C Kleijer, W J Van der Kraan, M Martin, J J Producer: 19930422 In: American journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Expression of melanocortin-5 receptor in secretory epithelia supports a functional role in exocrine and endocrine glands. [electronic resource] by van der Kraan, M Adan, R A Entwistle, M L Gispen, W H Burbach, J P Tatro, J B Producer: 19980508 In: Endocrinology vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Characterization of the sat operon in Streptococcus mutans: evidence for a role of Ffh in acid tolerance. [electronic resource] by Kremer, B H van der Kraan, M Crowley, P J Hamilton, I R Brady, L J Bleiweis, A S Producer: 20010503 In: Journal of bacteriology vol. 183 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Melanocortin receptors mediate alpha-MSH-induced stimulation of neurite outgrowth in neuro 2A cells. [electronic resource] by Adan, R A van der Kraan, M Doornbos, R P Bär, P R Burbach, J P Gispen, W H Producer: 19970206 In: Brain research. Molecular brain research vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Deletion of exon 18 is a frequent mutation in glycogen storage disease type II. [electronic resource] by Van der Kraan, M Kroos, M A Joosse, M Bijvoet, A G Verbeet, M P Kleijer, W J Reuser, A J Producer: 19941031 In: Biochemical and biophysical research communications vol. 203 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Expression of melanocortin receptors and pro-opiomelanocortin in the rat spinal cord in relation to neurotrophic effects of melanocortins. [electronic resource] by van der Kraan, M Tatro, J B Entwistle, M L Brakkee, J H Burbach, J P Adan, R A Gispen, W H Producer: 19990219 In: Brain research. Molecular brain research vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Homozygous deletion of exon 18 leads to degradation of the lysosomal alpha-glucosidase precursor and to the infantile form of glycogen storage disease type II. [electronic resource] by Ausems, M G Kroos, M A Van der Kraan, M Smeitink, J A Kleijer, W J Ploos van Amstel, H K Reuser, A J Producer: 19970122 In: Clinical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Prenatal diagnosis of glycogen storage disease type II: enzyme assay or mutation analysis? [electronic resource] by Kleijer, W J van der Kraan, M Kroos, M A Groener, J E van Diggelen, O P Reuser, A J van der Ploeg, A T Producer: 19951130 In: Pediatric research vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	[Estimate of the number of new patients with type 2 diabetes mellitus in the Netherlands: at least 65,000 per year in the age group of 50 years and above]. [electronic resource] by Dekker, J M van der Kraan, M Nijpels, G de Vegt, F Kostense, P J Stehouwer, C D A Bouter, L M Heine, R J Producer: 20031211 In: Nederlands tijdschrift voor geneeskunde vol. 147 Availability: No items available. Save to lists Add to cart (remove)
	15.	[Finnish questionnaire reasonably good predictor of the incidence of diabetes in The Netherlands]. [electronic resource] by Alssema, M Feskens, E J M Bakker, S J L Gansevoort, R T Boer, J M A Heine, R J Nijpels, G Stehouwer, C D A van der Kraan, M Dekker, J M Producer: 20081229 In: Nederlands tijdschrift voor geneeskunde vol. 152 Availability: No items available. Save to lists Add to cart (remove)
	16.	Prevalent mutations in the GALC gene of patients with Krabbe disease of Dutch and other European origin. [electronic resource] by Kleijer, W J Keulemans, J L van der Kraan, M Geilen, G G van der Helm, R M Rafi, M A Luzi, P Wenger, D A Halley, D J van Diggelen, O P Producer: 19971014 In: Journal of inherited metabolic disease vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Glycogen storage disease type II: frequency of three common mutant alleles and their associated clinical phenotypes studied in 121 patients. [electronic resource] by Kroos, M A Van der Kraan, M Van Diggelen, O P Kleijer, W J Reuser, A J Van den Boogaard, M J Ausems, M G Ploos van Amstel, H K Poenaru, L Nicolino, M Producer: 19960228 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)