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	1.	PCR detection of a dinucleotide repeat in the human histidine-rich glycoprotein (HRG) gene. [electronic resource] by Hennis, B C Havelaar, A C Kluft, C Producer: 19930617 In: Human molecular genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Lysosomal transport disorders. [electronic resource] by Mancini, G M Havelaar, A C Verheijen, F W Producer: 20001109 In: Journal of inherited metabolic disease vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Transport of organic anions by the lysosomal sialic acid transporter: a functional approach towards the gene for sialic acid storage disease. [electronic resource] by Havelaar, A C Beerens, C E Mancini, G M Verheijen, F W Producer: 19990507 In: FEBS letters vol. 446 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Purification of the lysosomal sialic acid transporter. Functional characteristics of a monocarboxylate transporter. [electronic resource] by Havelaar, A C Mancini, G M Beerens, C E Souren, R M Verheijen, F W Producer: 19990126 In: The Journal of biological chemistry vol. 273 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Fibroblast silver loading for the diagnosis of Menkes disease. [electronic resource] by Verheijen, F W Beerens, C E Havelaar, A C Kleijer, W J Mancini, G M Producer: 19990105 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Characterization of a heavy metal ion transporter in the lysosomal membrane. [electronic resource] by Havelaar, A C de Gast, I L Snijders, S Beerens, C E Mancini, G M Verheijen, F W Producer: 19981112 In: FEBS letters vol. 436 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	NPT4, a new microsomal phosphate transporter: mutation analysis in glycogen storage disease type Ic. [electronic resource] by Melis, D Havelaar, A C Verbeek, E Smit, G P A Benedetti, A Mancini, G M S Verheijen, F Producer: 20050505 In: Journal of inherited metabolic disease vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Interindividual and intraindividual variability in plasma fibrinogen, TPA antigen, PAI activity, and CRP in healthy, young volunteers and patients with angina pectoris. [electronic resource] by de Maat, M P de Bart, A C Hennis, B C Meijer, P Havelaar, A C Mulder, P G Kluft, C Producer: 19961024 In: Arteriosclerosis, thrombosis, and vascular biology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A role for the transient increase of cytoplasmic free calcium in cell rescue after photodynamic treatment. [electronic resource] by Penning, L C Rasch, M H Ben-Hur, E Dubbelman, T M Havelaar, A C Van der Zee, J Van Steveninck, J Producer: 19920921 In: Biochimica et biophysica acta vol. 1107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases. [electronic resource] by Verheijen, F W Verbeek, E Aula, N Beerens, C E Havelaar, A C Joosse, M Peltonen, L Aula, P Galjaard, H van der Spek, P J Mancini, G M Producer: 19991220 In: Nature genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)