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	1.	The effect of a single base pair deletion (delta T525) and a C1634T missense mutation (pro545leu) on the expression of lysosomal alpha-glucosidase in patients with glycogen storage disease type II. [electronic resource] by Hermans, M M De Graaff, E Kroos, M A Mohkamsing, S Eussen, B J Joosse, M Willemsen, R Kleijer, W J Oostra, B A Reuser, A J Producer: 19950413 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome. [electronic resource] by Wouters, C H Meijers-Heijboer, H J Eussen, B J van der Heide, A A van Luijk, R B van Drunen, E Beverloo, B B Visscher, F Van Hemel, J O Producer: 20010913 In: American journal of medical genetics vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Identification of a homozygous deletion at 8p12-21 in a human prostate cancer xenograft. [electronic resource] by Van Alewijk, D C Van der Weiden, M M Eussen, B J Van Den Andel-Thijssen, L D Ehren-van Eekelen, C C König, J J van Steenbrugge, G J Dinjens, W N Trapman, J Producer: 19990604 In: Genes, chromosomes & cancer vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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