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

S J Hebbring

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

Pageof 1
Sort By:
Cytogenetic and Genome Research|March 17, 2009
Sulfotransferase gene copy number variation: pharmacogenetics and functionS J Hebbring, A M Moyer, R M Weinshilboum
Genes and Immunity|February 9, 2013
A PheWAS approach in studying HLA-DRB1*1501S J Hebbring, S J Schrodi, Z Ye, et al.
American Journal of Human Genetics|February 4, 2003
Confirmation of linkage of prostate cancer aggressiveness with chromosome 19qS L Slager, D J Schaid, J M Cunningham, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 21, 2005
SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathiesC J Klein, Y Wu, K E Kruckeberg, et al.
Neurology|April 12, 2003
The gene for HMSN2C maps to 12q23-24: a region of neuromuscular disordersC J Klein, J M Cunningham, E J Atkinson, et al.
Pageof 1

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

Sort By:
Pageof 1
Cytogenetic and Genome Research|March 17, 2009
Sulfotransferase gene copy number variation: pharmacogenetics and functionS J Hebbring, A M Moyer, R M Weinshilboum
Genes and Immunity|February 9, 2013
A PheWAS approach in studying HLA-DRB1*1501S J Hebbring, S J Schrodi, Z Ye, et al.
American Journal of Human Genetics|February 4, 2003
Confirmation of linkage of prostate cancer aggressiveness with chromosome 19qS L Slager, D J Schaid, J M Cunningham, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 21, 2005
SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathiesC J Klein, Y Wu, K E Kruckeberg, et al.
Neurology|April 12, 2003
The gene for HMSN2C maps to 12q23-24: a region of neuromuscular disordersC J Klein, J M Cunningham, E J Atkinson, et al.
Pageof 1