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

L Ozelius

Showing results (11-20 of 32) with videos related to

Pageof 4
Sort By:
Human Mutation|October 26, 1999
Analysis of both TSC1 and TSC2 for germline mutations in 126 unrelated patients with tuberous sclerosisY Niida, N Lawrence-Smith, A Banwell, et al.
Clinical Genetics|February 1, 1994
The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9qJ Wahlström, L Ozelius, P Kramer, et al.
Human Mutation|November 26, 1998
Exon scanning of the entire TSC2 gene for germline mutations in 40 unrelated patients with tuberous sclerosisR L Beauchamp, A Banwell, P McNamara, et al.
American Journal of Human Genetics|August 1, 1991
Torsion dystonia genes in two populations confined to a small region on chromosome 9q32-34D J Kwiatkowski, L Ozelius, P L Kramer, et al.
Human Genetics|July 1, 1991
Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystoniaD Schuback, P Kramer, L Ozelius, et al.
Neurology|December 1, 1992
A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigationsM A Mikati, H Maguire, C F Barlow, et al.
Genomics|July 1, 1988
Human monoamine oxidase gene (MAOA): chromosome position (Xp21-p11) and DNA polymorphismL Ozelius, Y P Hsu, G Bruns, et al.
Journal of Neurogenetics|May 1, 1986
Linkage analysis in a family with dominantly inherited torsion dystonia: exclusion of the pro-opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphismsX O Breakefield, S B Bressman, P L Kramer, et al.
Annals of Human Genetics|March 30, 2000
Report and abstracts of the Sixth International Workshop on chromosome 9B P Chadwick, L J Campbell, C L Jackson, et al.
American Journal of Human Genetics|January 1, 1993
Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16W Yan, R M Boustany, C Konradi, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Human Mutation|October 26, 1999
Analysis of both TSC1 and TSC2 for germline mutations in 126 unrelated patients with tuberous sclerosisY Niida, N Lawrence-Smith, A Banwell, et al.
Clinical Genetics|February 1, 1994
The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9qJ Wahlström, L Ozelius, P Kramer, et al.
Human Mutation|November 26, 1998
Exon scanning of the entire TSC2 gene for germline mutations in 40 unrelated patients with tuberous sclerosisR L Beauchamp, A Banwell, P McNamara, et al.
American Journal of Human Genetics|August 1, 1991
Torsion dystonia genes in two populations confined to a small region on chromosome 9q32-34D J Kwiatkowski, L Ozelius, P L Kramer, et al.
Human Genetics|July 1, 1991
Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystoniaD Schuback, P Kramer, L Ozelius, et al.
Neurology|December 1, 1992
A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigationsM A Mikati, H Maguire, C F Barlow, et al.
Genomics|July 1, 1988
Human monoamine oxidase gene (MAOA): chromosome position (Xp21-p11) and DNA polymorphismL Ozelius, Y P Hsu, G Bruns, et al.
Journal of Neurogenetics|May 1, 1986
Linkage analysis in a family with dominantly inherited torsion dystonia: exclusion of the pro-opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphismsX O Breakefield, S B Bressman, P L Kramer, et al.
Annals of Human Genetics|March 30, 2000
Report and abstracts of the Sixth International Workshop on chromosome 9B P Chadwick, L J Campbell, C L Jackson, et al.
American Journal of Human Genetics|January 1, 1993
Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16W Yan, R M Boustany, C Konradi, et al.
Pageof 4