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

K E Davies

Showing results (1-10 of 316) with videos related to

Pageof 32
Sort By:
Human Genetics|January 1, 1981
The application of DNA recombinant technology to the analysis of the human genome and genetic diseaseK E Davies
Nature|March 5, 1992
Human genetics. The costs of instabilityK E Davies
American Journal of Medical Genetics|January 1, 1986
DNA studies of X-linked mental retardation associated with a fragile site at Xq27K E Davies
Disease Markers|March 1, 1987
Significant progress in Duchenne muscular dystrophyK E Davies
Neuromuscular Disorders : NMD|August 6, 2005
Regulation of utrophin in transgenic miceK E Davies
Neuromuscular Disorders : NMD|February 3, 1998
Challenges in Duchenne muscular dystrophyK E Davies
Journal of Medical Genetics|August 1, 1985
Molecular genetics of the human X chromosomeK E Davies
Current Opinion in Neurology|April 1, 1997
Fragile X syndromeL Chakrabarti, K E Davies
Horizons in Biochemistry and Biophysics|January 1, 1986
Towards a complete linkage map of the human X chromosomeK E Davies, R Williamson
Seminars in Neurology|July 10, 2001
Spinal muscular atrophyK Talbot, K E Davies
Pageof 32

Showing results (1-10 of 316) with videos related to

Sort By:
Pageof 32
Human Genetics|January 1, 1981
The application of DNA recombinant technology to the analysis of the human genome and genetic diseaseK E Davies
Nature|March 5, 1992
Human genetics. The costs of instabilityK E Davies
American Journal of Medical Genetics|January 1, 1986
DNA studies of X-linked mental retardation associated with a fragile site at Xq27K E Davies
Disease Markers|March 1, 1987
Significant progress in Duchenne muscular dystrophyK E Davies
Neuromuscular Disorders : NMD|August 6, 2005
Regulation of utrophin in transgenic miceK E Davies
Neuromuscular Disorders : NMD|February 3, 1998
Challenges in Duchenne muscular dystrophyK E Davies
Journal of Medical Genetics|August 1, 1985
Molecular genetics of the human X chromosomeK E Davies
Current Opinion in Neurology|April 1, 1997
Fragile X syndromeL Chakrabarti, K E Davies
Horizons in Biochemistry and Biophysics|January 1, 1986
Towards a complete linkage map of the human X chromosomeK E Davies, R Williamson
Seminars in Neurology|July 10, 2001
Spinal muscular atrophyK Talbot, K E Davies
Pageof 32