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

E G Murphy

Showing results (21-30 of 28) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 28 results.
Neuropsychologia|January 1, 1988
Recognition memory of item, associative and serial-order information after temporal lobectomy for seizure disorderM Dennis, K Farrell, H J Hoffman, et al.
American Journal of Human Genetics|February 1, 1991
Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophinD E Bulman, E G Murphy, E E Zubrzycka-Gaarn, et al.
Journal of Child Neurology|April 1, 1991
Infant-onset progressive myoclonus epilepsyM G Harbord, P A Hwang, B H Robinson, et al.
Muscle & Nerve|September 1, 1979
Serum creatine kinase and pyruvate kinase in Duchenne muscular dystrophy carrier detectionM E Percy, L S Chang, E G Murphy, et al.
Journal of Medical Genetics|June 1, 1988
Partial gene duplication in Duchenne and Becker muscular dystrophiesX Y Hu, A H Burghes, P N Ray, et al.
Neurology|August 1, 1992
Linkage analysis of candidate loci in autosomal dominant myotonia congenitaJ A Abdalla, W L Casley, A J Hudson, et al.
American Journal of Human Genetics|September 1, 1992
Linkage of Thomsen disease to the T-cell-receptor beta (TCRB) locus on chromosome 7q35J A Abdalla, W L Casley, H K Cousin, et al.
American Journal of Human Genetics|October 1, 1989
Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) geneE F Gillard, J S Chamberlain, E G Murphy, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Neuropsychologia|January 1, 1988
Recognition memory of item, associative and serial-order information after temporal lobectomy for seizure disorderM Dennis, K Farrell, H J Hoffman, et al.
American Journal of Human Genetics|February 1, 1991
Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophinD E Bulman, E G Murphy, E E Zubrzycka-Gaarn, et al.
Journal of Child Neurology|April 1, 1991
Infant-onset progressive myoclonus epilepsyM G Harbord, P A Hwang, B H Robinson, et al.
Muscle & Nerve|September 1, 1979
Serum creatine kinase and pyruvate kinase in Duchenne muscular dystrophy carrier detectionM E Percy, L S Chang, E G Murphy, et al.
Journal of Medical Genetics|June 1, 1988
Partial gene duplication in Duchenne and Becker muscular dystrophiesX Y Hu, A H Burghes, P N Ray, et al.
Neurology|August 1, 1992
Linkage analysis of candidate loci in autosomal dominant myotonia congenitaJ A Abdalla, W L Casley, A J Hudson, et al.
American Journal of Human Genetics|September 1, 1992
Linkage of Thomsen disease to the T-cell-receptor beta (TCRB) locus on chromosome 7q35J A Abdalla, W L Casley, H K Cousin, et al.
American Journal of Human Genetics|October 1, 1989
Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) geneE F Gillard, J S Chamberlain, E G Murphy, et al.
Pageof 3