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S Bunge

Showing results (11-20 of 28) with videos related to

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American Journal of Human Genetics|December 1, 1996
Mucopolysaccharidosis type II (Hunter syndrome): mutation "hot spots" in the iduronate-2-sulfatase geneM Rathmann, S Bunge, M Beck, et al.
Human Molecular Genetics|August 1, 1992
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)S Bunge, C Steglich, M Beck, et al.
Prenatal Diagnosis|September 1, 1994
Prenatal diagnosis and carrier detection in mucopolysaccharidosis type II by mutation analysis. A 47,XXY male heterozygous for a missense point mutationS Bunge, C Steglich, P Lorenz, et al.
Human Mutation|January 1, 1995
Mutations of the iduronate-2-sulfatase gene in 12 Polish patients with mucopolysaccharidosis type II (Hunter syndrome)E Popowska, M Rathmann, A Tylki-Szymanska, et al.
Biochimica Et Biophysica Acta|September 28, 1998
Genotype-phenotype correlations in mucopolysaccharidosis type I using enzyme kinetics, immunoquantification and in vitro turnover studiesS Bunge, P R Clements, S Byers, et al.
Human Mutation|January 1, 1995
Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implicationsH S Scott, S Bunge, A Gal, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Homologous nonallelic recombinations between the iduronate-sulfatase gene and pseudogene cause various intragenic deletions and inversions in patients with mucopolysaccharidosis type IIS Bunge, M Rathmann, C Steglich, et al.
Journal of Medical Genetics|February 9, 1999
Mucopolysaccharidosis type IIIB (Sanfilippo B): identification of 18 novel alpha-N-acetylglucosaminidase gene mutationsS Bunge, A Knigge, C Steglich, et al.
Human Molecular Genetics|September 1, 1997
Novel mutations in Sanfilippo A syndrome: implications for enzyme functionB Weber, X H Guo, J E Wraith, et al.
Human Genetics|September 1, 1993
Molecular analysis in patients with mucopolysaccharidosis type II suggests that DXS466 maps within the Hunter geneC Steglich, S Bunge, T Hulsebos, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
American Journal of Human Genetics|December 1, 1996
Mucopolysaccharidosis type II (Hunter syndrome): mutation "hot spots" in the iduronate-2-sulfatase geneM Rathmann, S Bunge, M Beck, et al.
Human Molecular Genetics|August 1, 1992
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)S Bunge, C Steglich, M Beck, et al.
Prenatal Diagnosis|September 1, 1994
Prenatal diagnosis and carrier detection in mucopolysaccharidosis type II by mutation analysis. A 47,XXY male heterozygous for a missense point mutationS Bunge, C Steglich, P Lorenz, et al.
Human Mutation|January 1, 1995
Mutations of the iduronate-2-sulfatase gene in 12 Polish patients with mucopolysaccharidosis type II (Hunter syndrome)E Popowska, M Rathmann, A Tylki-Szymanska, et al.
Biochimica Et Biophysica Acta|September 28, 1998
Genotype-phenotype correlations in mucopolysaccharidosis type I using enzyme kinetics, immunoquantification and in vitro turnover studiesS Bunge, P R Clements, S Byers, et al.
Human Mutation|January 1, 1995
Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implicationsH S Scott, S Bunge, A Gal, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Homologous nonallelic recombinations between the iduronate-sulfatase gene and pseudogene cause various intragenic deletions and inversions in patients with mucopolysaccharidosis type IIS Bunge, M Rathmann, C Steglich, et al.
Journal of Medical Genetics|February 9, 1999
Mucopolysaccharidosis type IIIB (Sanfilippo B): identification of 18 novel alpha-N-acetylglucosaminidase gene mutationsS Bunge, A Knigge, C Steglich, et al.
Human Molecular Genetics|September 1, 1997
Novel mutations in Sanfilippo A syndrome: implications for enzyme functionB Weber, X H Guo, J E Wraith, et al.
Human Genetics|September 1, 1993
Molecular analysis in patients with mucopolysaccharidosis type II suggests that DXS466 maps within the Hunter geneC Steglich, S Bunge, T Hulsebos, et al.
Pageof 3