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C P Morris

Showing results (21-30 of 85) with videos related to

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 21, 2001
The factor V HR2 haplotype: prevalence and association of the A4070G and A6755G polymorphismsN M Pecheniuk, C P Morris, T P Walsh, et al.
Brain Research|January 28, 1982
Developmental loss of a smooth muscle muscarinic receptor populationM F Crouch, C P Morris, T B Cheah, et al.
Nucleic Acids Research|November 25, 1991
PCR of a VNTR linked to mucopolysaccharidosis type I and Huntington diseaseH S Scott, P V Nelson, J J Hopwood, et al.
Genomics|August 1, 1992
Structure and sequence of the human alpha-L-iduronidase geneH S Scott, X H Guo, J J Hopwood, et al.
Genomics|September 1, 1993
Sequence of the human iduronate 2-sulfatase (IDS) geneP J Wilson, C A Meaney, J J Hopwood, et al.
American Journal of Medical Genetics|January 15, 1994
Mutation analysis of 28 Gaucher disease patients: the Australasian experienceB D Lewis, P V Nelson, E F Robertson, et al.
Human Molecular Genetics|January 1, 1994
Metachromatic leukodystrophy: a nonsense mutation (Q486X) in the arylsulphatase A (ARSA) geneJ S Harvey, W F Carey, P V Nelson, et al.
Human Mutation|January 1, 1994
Molecular genetics of metachromatic leukodystrophyV Gieselmann, J Zlotogora, A Harris, et al.
The Medical Journal of Australia|March 19, 1990
The frequency of the common (delta F508) cystic fibrosis mutation in the Australian populationP V Nelson, W F Carey, C P Morris, et al.
Nature|April 8, 1982
Neural regulation of muscarinic receptors in chick expansor secundariorum muscleR A Rush, M F Crouch, C P Morris, et al.
Pageof 9

Showing results (21-30 of 85) with videos related to

Sort By:
Pageof 9
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 21, 2001
The factor V HR2 haplotype: prevalence and association of the A4070G and A6755G polymorphismsN M Pecheniuk, C P Morris, T P Walsh, et al.
Brain Research|January 28, 1982
Developmental loss of a smooth muscle muscarinic receptor populationM F Crouch, C P Morris, T B Cheah, et al.
Nucleic Acids Research|November 25, 1991
PCR of a VNTR linked to mucopolysaccharidosis type I and Huntington diseaseH S Scott, P V Nelson, J J Hopwood, et al.
Genomics|August 1, 1992
Structure and sequence of the human alpha-L-iduronidase geneH S Scott, X H Guo, J J Hopwood, et al.
Genomics|September 1, 1993
Sequence of the human iduronate 2-sulfatase (IDS) geneP J Wilson, C A Meaney, J J Hopwood, et al.
American Journal of Medical Genetics|January 15, 1994
Mutation analysis of 28 Gaucher disease patients: the Australasian experienceB D Lewis, P V Nelson, E F Robertson, et al.
Human Molecular Genetics|January 1, 1994
Metachromatic leukodystrophy: a nonsense mutation (Q486X) in the arylsulphatase A (ARSA) geneJ S Harvey, W F Carey, P V Nelson, et al.
Human Mutation|January 1, 1994
Molecular genetics of metachromatic leukodystrophyV Gieselmann, J Zlotogora, A Harris, et al.
The Medical Journal of Australia|March 19, 1990
The frequency of the common (delta F508) cystic fibrosis mutation in the Australian populationP V Nelson, W F Carey, C P Morris, et al.
Nature|April 8, 1982
Neural regulation of muscarinic receptors in chick expansor secundariorum muscleR A Rush, M F Crouch, C P Morris, et al.
Pageof 9