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 G Nygaard

Showing results (41-50 of 49) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 49 results.
Annals of Neurology|November 30, 1999
Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31T G Nygaard, D Raymond, C Chen, et al.
Advances in Neurology|September 29, 1998
Molecular genetic analysis of LubagK C Wilhelmsen, C B Moskowitz, D E Weeks, et al.
Neurology|August 13, 2003
A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2L Palenzuela, A L Andreu, J Gàmez, et al.
American Journal of Human Genetics|April 25, 2000
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutationsG A Diaz, B D Gelb, N Risch, et al.
Neurology|January 5, 2002
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994T Lynch, M Sano, K S Marder, et al.
Annals of Neurology|October 1, 1996
Exclusion of the DYT1 locus in familial torticollisS B Bressman, T T Warner, L Almasy, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 1999
Primary torsion dystonia: the search for genes is not overP R Jarman, N del Grosso, E M Valente, et al.
Annals of Neurology|October 24, 1997
Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite familiesL Almasy, S B Bressman, D Raymond, et al.
Annals of Neurology|June 14, 2000
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutationsI Nishino, A Spinazzola, A Papadimitriou, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Annals of Neurology|November 30, 1999
Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31T G Nygaard, D Raymond, C Chen, et al.
Advances in Neurology|September 29, 1998
Molecular genetic analysis of LubagK C Wilhelmsen, C B Moskowitz, D E Weeks, et al.
Neurology|August 13, 2003
A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2L Palenzuela, A L Andreu, J Gàmez, et al.
American Journal of Human Genetics|April 25, 2000
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutationsG A Diaz, B D Gelb, N Risch, et al.
Neurology|January 5, 2002
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994T Lynch, M Sano, K S Marder, et al.
Annals of Neurology|October 1, 1996
Exclusion of the DYT1 locus in familial torticollisS B Bressman, T T Warner, L Almasy, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 1999
Primary torsion dystonia: the search for genes is not overP R Jarman, N del Grosso, E M Valente, et al.
Annals of Neurology|October 24, 1997
Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite familiesL Almasy, S B Bressman, D Raymond, et al.
Annals of Neurology|June 14, 2000
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutationsI Nishino, A Spinazzola, A Papadimitriou, et al.
Pageof 5