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

T N Mitchell

Showing results (11-20 of 14) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 14 results.
Neurology|April 14, 2004
Cognitive functioning in humans with mutations of the PAX6 geneP J Thompson, T N Mitchell, S L Free, et al.
Neuroimage|April 2, 2003
Quantitative MRI detects abnormalities in relatives of patients with epilepsy and malformations of cortical developmentM Merschhemke, T N Mitchell, S L Free, et al.
American Journal of Human Genetics|January 13, 2000
A novel locus for Leber congenital amaurosis maps to chromosome 6qS Dharmaraj, Y Li, J M Robitaille, et al.
Nature Genetics|June 30, 2001
PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humansS M Sisodiya, S L Free, K A Williamson, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Neurology|April 14, 2004
Cognitive functioning in humans with mutations of the PAX6 geneP J Thompson, T N Mitchell, S L Free, et al.
Neuroimage|April 2, 2003
Quantitative MRI detects abnormalities in relatives of patients with epilepsy and malformations of cortical developmentM Merschhemke, T N Mitchell, S L Free, et al.
American Journal of Human Genetics|January 13, 2000
A novel locus for Leber congenital amaurosis maps to chromosome 6qS Dharmaraj, Y Li, J M Robitaille, et al.
Nature Genetics|June 30, 2001
PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humansS M Sisodiya, S L Free, K A Williamson, et al.
Pageof 2