Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

N C Foulds

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
Analytical Chemistry|November 15, 1988
Immobilization of glucose oxidase in ferrocene-modified pyrrole polymersN C Foulds, C R Lowe
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|September 1, 1985
Biosensors: current applications and future potentialN C Foulds, C R Lowe
Molecular Syndromology|November 4, 2010
Persistent Fetal Vasculature and Severe Protein C DeficiencyA G L Douglas, H Rafferty, P Hodgkins, et al.
Neurology|April 7, 2010
Pseudodominant inheritance of spastic ataxia of Charlevoix-SaguenayA Terracciano, N C Foulds, A Ditchfield, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Detection of 53 FBN1 mutations (41 novel and 12 recurrent) and genotype-phenotype correlations in 113 unrelated probands referred with Marfan syndrome, or a related fibrillinopathyC L S Turner, H Emery, A L Collins, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Analytical Chemistry|November 15, 1988
Immobilization of glucose oxidase in ferrocene-modified pyrrole polymersN C Foulds, C R Lowe
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|September 1, 1985
Biosensors: current applications and future potentialN C Foulds, C R Lowe
Molecular Syndromology|November 4, 2010
Persistent Fetal Vasculature and Severe Protein C DeficiencyA G L Douglas, H Rafferty, P Hodgkins, et al.
Neurology|April 7, 2010
Pseudodominant inheritance of spastic ataxia of Charlevoix-SaguenayA Terracciano, N C Foulds, A Ditchfield, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Detection of 53 FBN1 mutations (41 novel and 12 recurrent) and genotype-phenotype correlations in 113 unrelated probands referred with Marfan syndrome, or a related fibrillinopathyC L S Turner, H Emery, A L Collins, et al.
Pageof 1