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

R P Bruyn

Showing results (21-30 of 23) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 23 results.
Neuroradiology|January 1, 1993
SPECT, CT and MRI in a Turkish family with Huntington's diseaseR P Bruyn, G Hageman, J A Geelen, et al.
Human Genetics|April 1, 1994
Pure hereditary spastic paraparesis: an exclusion map covering more than 40% of the autosomal genomeJ C van Deutekom, R P Bruyn, N van den Boorn, et al.
Human Molecular Genetics|September 1, 1994
Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2pJ Hazan, B Fontaine, R P Bruyn, et al.
Pageof 3

Showing results (21-30 of 23) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 23 results.
Neuroradiology|January 1, 1993
SPECT, CT and MRI in a Turkish family with Huntington's diseaseR P Bruyn, G Hageman, J A Geelen, et al.
Human Genetics|April 1, 1994
Pure hereditary spastic paraparesis: an exclusion map covering more than 40% of the autosomal genomeJ C van Deutekom, R P Bruyn, N van den Boorn, et al.
Human Molecular Genetics|September 1, 1994
Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2pJ Hazan, B Fontaine, R P Bruyn, et al.
Pageof 3