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C P Morris

Showing results (31-40 of 85) with videos related to

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Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|July 27, 2001
Solid-phase amplification and detection: a single-tube diagnostic assay for infectious agentsM Somodevilla-Torres, P Timms, R Harris, et al.
American Journal of Human Genetics|June 1, 1997
Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndromeB C Paton, S E Heron, P V Nelson, et al.
Biochemistry International|May 1, 1991
Human N-acetylgalactosamine-4-sulphatase: protein maturation and isolation of genomic clonesT Litjens, C P Morris, G J Gibson, et al.
Genomics|August 1, 1994
Morquio A syndrome: cloning, sequence, and structure of the human N-acetylgalactosamine 6-sulfatase (GALNS) geneC P Morris, X H Guo, S Apostolou, et al.
Human Molecular Genetics|September 1, 1993
Multiple polymorphisms within the alpha-L-iduronidase gene (IDUA): implications for a role in modification of MPS-I disease phenotypeH S Scott, P V Nelson, T Litjens, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|February 21, 2015
Dysbindin (DTNBP1) variants are associated with hallucinations in schizophreniaS-Y Cheah, B R Lawford, R M Young, et al.
Biotechniques|December 4, 2001
Interrogation of multimeric DNA amplification products by competitive primer extension using bst DNA polymerase (large fragment)J Voisey, G J Hafner, C P Morris, et al.
Biochemical and Biophysical Research Communications|November 30, 1988
Human glucosamine-6-sulfatase cDNA reveals homology with steroid sulfataseD A Robertson, C Freeman, P V Nelson, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Gene diagnosis and carrier detection in Hunter syndrome by the iduronate-2-sulphatase cDNA probeA Gal, M Beck, A C Sewell, et al.
Human Genetics|June 1, 1988
Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14D A Robertson, D F Callen, E G Baker, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|July 27, 2001
Solid-phase amplification and detection: a single-tube diagnostic assay for infectious agentsM Somodevilla-Torres, P Timms, R Harris, et al.
American Journal of Human Genetics|June 1, 1997
Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndromeB C Paton, S E Heron, P V Nelson, et al.
Biochemistry International|May 1, 1991
Human N-acetylgalactosamine-4-sulphatase: protein maturation and isolation of genomic clonesT Litjens, C P Morris, G J Gibson, et al.
Genomics|August 1, 1994
Morquio A syndrome: cloning, sequence, and structure of the human N-acetylgalactosamine 6-sulfatase (GALNS) geneC P Morris, X H Guo, S Apostolou, et al.
Human Molecular Genetics|September 1, 1993
Multiple polymorphisms within the alpha-L-iduronidase gene (IDUA): implications for a role in modification of MPS-I disease phenotypeH S Scott, P V Nelson, T Litjens, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|February 21, 2015
Dysbindin (DTNBP1) variants are associated with hallucinations in schizophreniaS-Y Cheah, B R Lawford, R M Young, et al.
Biotechniques|December 4, 2001
Interrogation of multimeric DNA amplification products by competitive primer extension using bst DNA polymerase (large fragment)J Voisey, G J Hafner, C P Morris, et al.
Biochemical and Biophysical Research Communications|November 30, 1988
Human glucosamine-6-sulfatase cDNA reveals homology with steroid sulfataseD A Robertson, C Freeman, P V Nelson, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Gene diagnosis and carrier detection in Hunter syndrome by the iduronate-2-sulphatase cDNA probeA Gal, M Beck, A C Sewell, et al.
Human Genetics|June 1, 1988
Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14D A Robertson, D F Callen, E G Baker, et al.
Pageof 9