Your search returned 7 results.

Results
	1.	Anti-surface antibodies to Entamoeba histolytica and their role in complement lysis. [electronic resource] by Trissl, D Müller, R Ries, R Rathmann, M Producer: 19870626 In: Archivos de investigacion medica vol. 17 Suppl 1 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Microwave volumetry of the extremities: a technical measuring alternative to the noninvasive venous occlusion test]. [electronic resource] by Blazek, V Schmitt, H J Schultz-Ehrenburg, U Rathmann, M Producer: 19951102 In: Biomedizinische Technik. Biomedical engineering vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	3.	Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28. [electronic resource] by Rathmann, M Bunge, S Steglich, C Schwinger, E Gal, A Producer: 19950203 In: Human genetics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Mucopolysaccharidosis type II (Hunter syndrome): mutation "hot spots" in the iduronate-2-sulfatase gene. [electronic resource] by Rathmann, M Bunge, S Beck, M Kresse, H Tylki-Szymanska, A Gal, A Producer: 19970114 In: American journal of human genetics vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	5.	Mutations of the iduronate-2-sulfatase gene in 12 Polish patients with mucopolysaccharidosis type II (Hunter syndrome). [electronic resource] by Popowska, E Rathmann, M Tylki-Szymanska, A Bunge, S Steglich, C Schwinger, E Gal, A Producer: 19950530 In: Human mutation vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Homologous nonallelic recombinations between the iduronate-sulfatase gene and pseudogene cause various intragenic deletions and inversions in patients with mucopolysaccharidosis type II. [electronic resource] by Bunge, S Rathmann, M Steglich, C Bondeson, M L Tylki-Szymanska, A Popowska, E Gal, A Producer: 19990107 In: European journal of human genetics : EJHG vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy. [electronic resource] by Gu, S M Thompson, D A Srikumari, C R Lorenz, B Finckh, U Nicoletti, A Murthy, K R Rathmann, M Kumaramanickavel, G Denton, M J Gal, A Producer: 19971114 In: Nature genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)