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	1.	Identification of an alternative transcript from the human iduronate-2-sulfatase (IDS) gene. [electronic resource] by Malmgren, H Carlberg, B M Pettersson, U Bondeson, M L Producer: 19960201 In: Genomics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Presence of an IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndrome. [electronic resource] by Bondeson, M L Malmgren, H Dahl, N Carlberg, B M Pettersson, U Producer: 19960201 In: European journal of human genetics : EJHG vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Analysis of a 43.6 kb deletion in a patient with Hunter syndrome (MPSII): identification of a fusion transcript including sequences from the gene W and the IDS gene. [electronic resource] by Lagerstedt, K Carlberg, B M Karimi-Nejad, R Kleijer, W J Bondeson, M L Producer: 20000516 In: Human mutation vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome. [electronic resource] by Bondeson, M L Dahl, N Malmgren, H Kleijer, W J Tönnesen, T Carlberg, B M Pettersson, U Producer: 19950911 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Double-strand breaks may initiate the inversion mutation causing the Hunter syndrome. [electronic resource] by Lagerstedt, K Karsten, S L Carlberg, B M Kleijer, W J Tönnesen, T Pettersson, U Bondeson, M L Producer: 19970715 In: Human molecular genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Identification of 9 novel IDS gene mutations in 19 unrelated Hunter syndrome (mucopolysaccharidosis Type II) patients. Mutations in brief no. 202. Online. [electronic resource] by Karsten, S L Voskoboeva, E Carlberg, B M Kleijer, W J Tsnnesen, T Pettersson, U Bondeson, M L Producer: 20000208 In: Human mutation vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Two distinct deletions in the IDS gene and the gene W: a novel type of mutation associated with the Hunter syndrome. [electronic resource] by Karsten, S L Lagerstedt, K Carlberg, B M Kleijer, W J Zaremba, J Van Diggelen, O P Czartoryska, B Pettersson, U Bondeson, M L Producer: 19970925 In: Genomics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)