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

S R Shaw

Showing results (51-60 of 54) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 54 results.
Clinical Radiology|June 9, 2007
Multi-detector row CT coronary angiography in patients with cardiomyopathy -- initial single-centre experienceN E Manghat, G J Morgan-Hughes, S R Shaw, et al.
Cladistics : the International Journal of the Willi Hennig Society|December 21, 2021
PHYLOGENY OF THE SUBFAMILIES OF THE FAMILY BRACONIDAE (HYMENOPTERA: ICHNEUMONOIDEA): A REASSESSMENTR A Wharton, S R Shaw, M J Sharkey, et al.
American Journal of Medical Genetics|June 8, 2001
22q13 deletion syndromeM C Phelan, R C Rogers, R A Saul, et al.
Journal of Medical Genetics|August 16, 2003
Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptomsH L Wilson, A C C Wong, S R Shaw, et al.
Pageof 6

Showing results (51-60 of 54) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 54 results.
Clinical Radiology|June 9, 2007
Multi-detector row CT coronary angiography in patients with cardiomyopathy -- initial single-centre experienceN E Manghat, G J Morgan-Hughes, S R Shaw, et al.
Cladistics : the International Journal of the Willi Hennig Society|December 21, 2021
PHYLOGENY OF THE SUBFAMILIES OF THE FAMILY BRACONIDAE (HYMENOPTERA: ICHNEUMONOIDEA): A REASSESSMENTR A Wharton, S R Shaw, M J Sharkey, et al.
American Journal of Medical Genetics|June 8, 2001
22q13 deletion syndromeM C Phelan, R C Rogers, R A Saul, et al.
Journal of Medical Genetics|August 16, 2003
Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptomsH L Wilson, A C C Wong, S R Shaw, et al.
Pageof 6