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C P Morris

Showing results (1-10 of 85) with videos related to

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Molecular Biology & Medicine|October 1, 1990
The mucopolysaccharidoses. Diagnosis, molecular genetics and treatmentJ J Hopwood, C P Morris
Molecular Biology Reports|August 31, 1979
The terminal structures of feather keratin mRNAC P Morris, G E Rogers
Human Molecular Genetics|June 1, 1994
A nonsense mutation (R220X) in the alpha-galactosidase A gene detected in a female carrier of Fabry diseaseC Meaney, L C Blanch, C P Morris
Biochemical and Biophysical Research Communications|May 29, 1987
Yeast pyruvate carboxylase: gene isolationC P Morris, F Lim, J C Wallace
Human Mutation|January 1, 1996
A sensitive mutation screening strategy for Fabry disease: detection of nine mutations in the alpha-galactosidase A geneL C Blanch, C Meaney, C P Morris
Human Genetics|February 1, 1991
Identification of a cystic fibrosis mutation: deletion of isoleucine506P V Nelson, W F Carey, C P Morris
Lancet (London, England)|December 8, 1990
Gene amplification directly from Guthrie blood spotsP V Nelson, W F Carey, C P Morris
Human Genetics|May 1, 1991
Population frequency of the arylsulphatase A pseudo-deficiency alleleP V Nelson, W F Carey, C P Morris
Human Molecular Genetics|July 21, 1998
Importance of the glycosylation and polyadenylation variants in metachromatic leukodystrophy pseudodeficiency phenotypeJ S Harvey, W F Carey, C P Morris
Archives of Biochemistry and Biophysics|October 1, 1987
Pyruvate carboxylase in the yeast pyc mutantF Lim, M Rohde, C P Morris, et al.
Pageof 9

Showing results (1-10 of 85) with videos related to

Sort By:
Pageof 9
Molecular Biology & Medicine|October 1, 1990
The mucopolysaccharidoses. Diagnosis, molecular genetics and treatmentJ J Hopwood, C P Morris
Molecular Biology Reports|August 31, 1979
The terminal structures of feather keratin mRNAC P Morris, G E Rogers
Human Molecular Genetics|June 1, 1994
A nonsense mutation (R220X) in the alpha-galactosidase A gene detected in a female carrier of Fabry diseaseC Meaney, L C Blanch, C P Morris
Biochemical and Biophysical Research Communications|May 29, 1987
Yeast pyruvate carboxylase: gene isolationC P Morris, F Lim, J C Wallace
Human Mutation|January 1, 1996
A sensitive mutation screening strategy for Fabry disease: detection of nine mutations in the alpha-galactosidase A geneL C Blanch, C Meaney, C P Morris
Human Genetics|February 1, 1991
Identification of a cystic fibrosis mutation: deletion of isoleucine506P V Nelson, W F Carey, C P Morris
Lancet (London, England)|December 8, 1990
Gene amplification directly from Guthrie blood spotsP V Nelson, W F Carey, C P Morris
Human Genetics|May 1, 1991
Population frequency of the arylsulphatase A pseudo-deficiency alleleP V Nelson, W F Carey, C P Morris
Human Molecular Genetics|July 21, 1998
Importance of the glycosylation and polyadenylation variants in metachromatic leukodystrophy pseudodeficiency phenotypeJ S Harvey, W F Carey, C P Morris
Archives of Biochemistry and Biophysics|October 1, 1987
Pyruvate carboxylase in the yeast pyc mutantF Lim, M Rohde, C P Morris, et al.
Pageof 9