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

P L Kramer

Showing results (21-30 of 49) with videos related to

Pageof 5
Sort By:
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.
Genomics|December 1, 1992
The CEPH consortium linkage map of human chromosome 15qA M Bowcock, R I Barnes, R L White, et al.
Advances in Neurology|September 29, 1998
Clinical-genetic spectrum of primary dystoniaS B Bressman, D de Leon, D Raymond, et al.
Nature Photonics|June 8, 2026
Strong ultrafast nonlinear optical response from megaelectronvolt electrons in semiconductorsD Jeong, T R Hopper, Y Kim, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2005
Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new familyK Kabakci, K Isbruch, K Schilling, et al.
Annals of Neurology|November 1, 1994
Dystonia in Ashkenazi Jews: clinical characterization of a founder mutationS B Bressman, D de Leon, P L Kramer, et al.
Annals of Neurology|February 1, 1990
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34P L Kramer, D de Leon, L Ozelius, et al.
American Journal of Human Genetics|September 1, 1994
The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-JewsP L Kramer, G A Heiman, T Gasser, et al.
Neurology|June 1, 1997
Secondary dystonia and the DYTI geneS B Bressman, D de Leon, D Raymond, et al.
Molecular Biology & Medicine|December 1, 1986
DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomiaX O Breakefield, L Ozelius, M A Bothwell, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
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.
Genomics|December 1, 1992
The CEPH consortium linkage map of human chromosome 15qA M Bowcock, R I Barnes, R L White, et al.
Advances in Neurology|September 29, 1998
Clinical-genetic spectrum of primary dystoniaS B Bressman, D de Leon, D Raymond, et al.
Nature Photonics|June 8, 2026
Strong ultrafast nonlinear optical response from megaelectronvolt electrons in semiconductorsD Jeong, T R Hopper, Y Kim, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2005
Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new familyK Kabakci, K Isbruch, K Schilling, et al.
Annals of Neurology|November 1, 1994
Dystonia in Ashkenazi Jews: clinical characterization of a founder mutationS B Bressman, D de Leon, P L Kramer, et al.
Annals of Neurology|February 1, 1990
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34P L Kramer, D de Leon, L Ozelius, et al.
American Journal of Human Genetics|September 1, 1994
The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-JewsP L Kramer, G A Heiman, T Gasser, et al.
Neurology|June 1, 1997
Secondary dystonia and the DYTI geneS B Bressman, D de Leon, D Raymond, et al.
Molecular Biology & Medicine|December 1, 1986
DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomiaX O Breakefield, L Ozelius, M A Bothwell, et al.
Pageof 5