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S Bunge

Showing results (21-30 of 28) with videos related to

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Human Mutation|January 1, 1993
Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase geneJ J Hopwood, S Bunge, C P Morris, et al.
Journal of Inherited Metabolic Disease|January 24, 2002
Anderson-Fabry disease: clinical manifestations of disease in female heterozygotesC Whybra, C Kampmann, I Willers, et al.
Human Molecular Genetics|November 1, 1993
Iduronate-2-sulfatase gene mutations in 16 patients with mucopolysaccharidosis type II (Hunter syndrome)S Bunge, C Steglich, C Zuther, et al.
Clinical Genetics|July 11, 1998
Clinical, biochemical and molecular findings in a two-generation Morquio A familyA Tylki-Szymańska, B Czartoryska, S Bunge, et al.
Human Molecular Genetics|June 1, 1994
Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common alpha-L-iduronidase mutations (W402X and Q70X) among European patientsS Bunge, W J Kleijer, C Steglich, et al.
Human Mutation|January 1, 1997
Identification of 16 sulfamidase gene mutations including the common R74C in patients with mucopolysaccharidosis type IIIA (Sanfilippo A)S Bunge, H Ince, C Steglich, et al.
Genomics|July 1, 1993
Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosaS Bunge, H Wedemann, D David, et al.
Human Mutation|January 1, 1997
Identification of 31 novel mutations in the N-acetylgalactosamine-6-sulfatase gene reveals excessive allelic heterogeneity among patients with Morquio A syndromeS Bunge, W J Kleijer, A Tylki-Szymanska, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Human Mutation|January 1, 1993
Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase geneJ J Hopwood, S Bunge, C P Morris, et al.
Journal of Inherited Metabolic Disease|January 24, 2002
Anderson-Fabry disease: clinical manifestations of disease in female heterozygotesC Whybra, C Kampmann, I Willers, et al.
Human Molecular Genetics|November 1, 1993
Iduronate-2-sulfatase gene mutations in 16 patients with mucopolysaccharidosis type II (Hunter syndrome)S Bunge, C Steglich, C Zuther, et al.
Clinical Genetics|July 11, 1998
Clinical, biochemical and molecular findings in a two-generation Morquio A familyA Tylki-Szymańska, B Czartoryska, S Bunge, et al.
Human Molecular Genetics|June 1, 1994
Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common alpha-L-iduronidase mutations (W402X and Q70X) among European patientsS Bunge, W J Kleijer, C Steglich, et al.
Human Mutation|January 1, 1997
Identification of 16 sulfamidase gene mutations including the common R74C in patients with mucopolysaccharidosis type IIIA (Sanfilippo A)S Bunge, H Ince, C Steglich, et al.
Genomics|July 1, 1993
Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosaS Bunge, H Wedemann, D David, et al.
Human Mutation|January 1, 1997
Identification of 31 novel mutations in the N-acetylgalactosamine-6-sulfatase gene reveals excessive allelic heterogeneity among patients with Morquio A syndromeS Bunge, W J Kleijer, A Tylki-Szymanska, et al.
Pageof 3