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

W G Wilson

Showing results (51-60 of 70) with videos related to

Pageof 7
Sort By:
Journal of Medical Genetics|December 1, 1983
Agenesis of the corpus callosum in two brothersW G Wilson, J M Kennaugh, J P Kugler, et al.
Virginia Medical|April 1, 1983
Fragile X-linked mental retardation, a new entity: case reportsT E Kelly, M A Shires, L Harris, et al.
Southern Medical Journal|December 1, 1988
Cytogenetic studies in couples with recurrent pregnancy lossD Sider, W G Wilson, K Sudduth, et al.
European Journal of Pediatrics|September 1, 1984
A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyW G Wilson, M B Cass, O Søvik, et al.
Plastic and Reconstructive Surgery|July 1, 1997
Distribution of organosilicon polymers in augmentation mammaplasties at autopsyJ J Barnard, E L Todd, W G Wilson, et al.
American Journal of Medical Genetics|October 1, 1989
"New" ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feetW G Wilson, K E Greer, A B Martof, et al.
American Journal of Medical Genetics|September 15, 1992
Deletion (14) (q24.3q32.1): evidence for a distinct clinical phenotypeS A Karnitis, K Burns, K W Sudduth, et al.
American Journal of Medical Genetics|October 1, 1989
Holoprosencephaly and interstitial deletion of 2(p2101p2109)W G Wilson, D E Shanks, K W Sudduth, et al.
Cytogenetics and Cell Genetics|January 1, 1982
Human chromosome 2 rod/ring mosaicism: probable origin by prezygotic breakage and intrachromosomal exchangeH E Wyandt, R Kasprzak, A Lamb, et al.
American Journal of Medical Genetics|January 1, 1990
Neonatal progeroid syndrome: more than one disease?J I Hagadorn, W G Wilson, W A Hogge, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|December 1, 1983
Agenesis of the corpus callosum in two brothersW G Wilson, J M Kennaugh, J P Kugler, et al.
Virginia Medical|April 1, 1983
Fragile X-linked mental retardation, a new entity: case reportsT E Kelly, M A Shires, L Harris, et al.
Southern Medical Journal|December 1, 1988
Cytogenetic studies in couples with recurrent pregnancy lossD Sider, W G Wilson, K Sudduth, et al.
European Journal of Pediatrics|September 1, 1984
A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyW G Wilson, M B Cass, O Søvik, et al.
Plastic and Reconstructive Surgery|July 1, 1997
Distribution of organosilicon polymers in augmentation mammaplasties at autopsyJ J Barnard, E L Todd, W G Wilson, et al.
American Journal of Medical Genetics|October 1, 1989
"New" ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feetW G Wilson, K E Greer, A B Martof, et al.
American Journal of Medical Genetics|September 15, 1992
Deletion (14) (q24.3q32.1): evidence for a distinct clinical phenotypeS A Karnitis, K Burns, K W Sudduth, et al.
American Journal of Medical Genetics|October 1, 1989
Holoprosencephaly and interstitial deletion of 2(p2101p2109)W G Wilson, D E Shanks, K W Sudduth, et al.
Cytogenetics and Cell Genetics|January 1, 1982
Human chromosome 2 rod/ring mosaicism: probable origin by prezygotic breakage and intrachromosomal exchangeH E Wyandt, R Kasprzak, A Lamb, et al.
American Journal of Medical Genetics|January 1, 1990
Neonatal progeroid syndrome: more than one disease?J I Hagadorn, W G Wilson, W A Hogge, et al.
Pageof 7