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 S Harper

Showing results (211-220 of 216) with videos related to

Pageof 22
Sort By:
You have reached the last page of results.This site can display upto 216 results.
Science (New York, N.Y.)|December 8, 1989
A new DNA marker tightly linked to the fragile X locus (FRAXA)G K Suthers, D F Callen, V J Hyland, et al.
Science (New York, N.Y.)|November 4, 1988
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophyS B Malhotra, K A Hart, H J Klamut, et al.
American Journal of Human Genetics|April 11, 2001
Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14M McEntagart, N Norton, H Williams, et al.
Genomics|August 1, 1989
Huntington disease: no evidence for locus heterogeneityP M Conneally, J L Haines, R E Tanzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1997
Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigreesM W Becher, D C Rubinsztein, J Leggo, et al.
American Journal of Human Genetics|July 1, 1996
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeatsD C Rubinsztein, J Leggo, R Coles, et al.
Pageof 22

Showing results (211-220 of 216) with videos related to

Sort By:
Pageof 22
You have reached the last page of results.This site can display upto 216 results.
Science (New York, N.Y.)|December 8, 1989
A new DNA marker tightly linked to the fragile X locus (FRAXA)G K Suthers, D F Callen, V J Hyland, et al.
Science (New York, N.Y.)|November 4, 1988
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophyS B Malhotra, K A Hart, H J Klamut, et al.
American Journal of Human Genetics|April 11, 2001
Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14M McEntagart, N Norton, H Williams, et al.
Genomics|August 1, 1989
Huntington disease: no evidence for locus heterogeneityP M Conneally, J L Haines, R E Tanzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1997
Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigreesM W Becher, D C Rubinsztein, J Leggo, et al.
American Journal of Human Genetics|July 1, 1996
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeatsD C Rubinsztein, J Leggo, R Coles, et al.
Pageof 22