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C P Morris

Showing results (51-60 of 85) with videos related to

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Human Genetics|April 1, 1989
Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphataseT Litjens, E G Baker, K R Beckmann, et al.
Genomics|December 1, 1992
An 86-bp VNTR within IDUA is the basis of the D4S111 polymorphic locusH S Scott, P V Nelson, M E MacDonald, et al.
Clinical Chemistry|July 27, 2001
Solid-phase amplification for detection of C282y and H63D hemochromatosis (HFE) gene mutationsM S Turner, S Penning, A Sharp, et al.
Human Mutation|January 1, 1994
Mutation analysis of 19 North American mucopolysaccharidosis type I patients: identification of two additional frequent mutationsL A Clarke, P V Nelson, C L Warrington, et al.
Nucleic Acids Research|October 26, 1987
Sequence of human 5-aminolevulinate synthase cDNAM J Bawden, I A Borthwick, H M Healy, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1990
Hunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNAP J Wilson, C P Morris, D S Anson, et al.
Human Genetics|June 1, 1991
The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulphatase gene (mucopolysaccharidosis II--Hunter syndrome)J E Wraith, A Cooper, M Thornley, et al.
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.
BMJ (Clinical Research Ed.)|May 25, 1991
Neonatal screening strategy for cystic fibrosis using immunoreactive trypsinogen and direct gene analysisE Ranieri, R G Ryall, C P Morris, et al.
American Journal of Human Genetics|January 1, 1993
The morquio A syndrome (mucopolysaccharidosis IVA) gene maps to 16q24.3E Baker, X H Guo, A M Orsborn, et al.
Pageof 9

Showing results (51-60 of 85) with videos related to

Sort By:
Pageof 9
Human Genetics|April 1, 1989
Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphataseT Litjens, E G Baker, K R Beckmann, et al.
Genomics|December 1, 1992
An 86-bp VNTR within IDUA is the basis of the D4S111 polymorphic locusH S Scott, P V Nelson, M E MacDonald, et al.
Clinical Chemistry|July 27, 2001
Solid-phase amplification for detection of C282y and H63D hemochromatosis (HFE) gene mutationsM S Turner, S Penning, A Sharp, et al.
Human Mutation|January 1, 1994
Mutation analysis of 19 North American mucopolysaccharidosis type I patients: identification of two additional frequent mutationsL A Clarke, P V Nelson, C L Warrington, et al.
Nucleic Acids Research|October 26, 1987
Sequence of human 5-aminolevulinate synthase cDNAM J Bawden, I A Borthwick, H M Healy, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1990
Hunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNAP J Wilson, C P Morris, D S Anson, et al.
Human Genetics|June 1, 1991
The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulphatase gene (mucopolysaccharidosis II--Hunter syndrome)J E Wraith, A Cooper, M Thornley, et al.
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.
BMJ (Clinical Research Ed.)|May 25, 1991
Neonatal screening strategy for cystic fibrosis using immunoreactive trypsinogen and direct gene analysisE Ranieri, R G Ryall, C P Morris, et al.
American Journal of Human Genetics|January 1, 1993
The morquio A syndrome (mucopolysaccharidosis IVA) gene maps to 16q24.3E Baker, X H Guo, A M Orsborn, et al.
Pageof 9