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

Roger E Stevenson

Showing results (11-20 of 158) with videos related to

Pageof 16
Sort By:
American Journal of Human Genetics|April 10, 2012
Fragile X and X-linked intellectual disability: four decades of discoveryHerbert A Lubs, Roger E Stevenson, Charles E Schwartz
American Journal of Medical Genetics. Part A|April 7, 2020
Fatal hyperkeratosis syndrome in four siblings due to dolichol kinase deficiencyBryan D Hall, Roger E Stevenson, Julie R Jones
American Journal of Medical Genetics. Part A|October 30, 2013
Malformations among the X-linked intellectual disability syndromesRoger E Stevenson, Charles E Schwartz, R Curtis Rogers
American Journal of Medical Genetics. Part A|August 5, 2011
Limb-body wall defect. Is there a defensible hypothesis and can it explain all the associated anomalies?Alasdair G W Hunter, Laurie H Seaver, Roger E Stevenson
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 25, 2008
Clinical geneticists in birth defects surveillance and epidemiology research programs: past, present and future rolesAngela E Lin, Sonja A Rasmussen, Angela Scheuerle, et al.
Neurogenetics|March 12, 2009
The impact of spermine synthase (SMS) mutations on brain morphologyShelli R Kesler, Charles Schwartz, Roger E Stevenson, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 15, 2011
Spermine synthase deficiency resulting in X-linked intellectual disability (Snyder-Robinson syndrome)Charles E Schwartz, Xaiojing Wang, Roger E Stevenson, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
X-linked intellectual disability update 2017Giovanni Neri, Charles E Schwartz, Herbert A Lubs, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 16, 2004
Neural tube defects and associated anomalies in South CarolinaRoger E Stevenson, Laurie H Seaver, Julianne S Collins, et al.
Ophthalmic Genetics|January 24, 2017
Ocular manifestations in the X-linked intellectual disability syndromesNatario L Couser, Maheer M Masood, Arthur S Aylsworth, et al.
Pageof 16

Showing results (11-20 of 158) with videos related to

Sort By:
Pageof 16
American Journal of Human Genetics|April 10, 2012
Fragile X and X-linked intellectual disability: four decades of discoveryHerbert A Lubs, Roger E Stevenson, Charles E Schwartz
American Journal of Medical Genetics. Part A|April 7, 2020
Fatal hyperkeratosis syndrome in four siblings due to dolichol kinase deficiencyBryan D Hall, Roger E Stevenson, Julie R Jones
American Journal of Medical Genetics. Part A|October 30, 2013
Malformations among the X-linked intellectual disability syndromesRoger E Stevenson, Charles E Schwartz, R Curtis Rogers
American Journal of Medical Genetics. Part A|August 5, 2011
Limb-body wall defect. Is there a defensible hypothesis and can it explain all the associated anomalies?Alasdair G W Hunter, Laurie H Seaver, Roger E Stevenson
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 25, 2008
Clinical geneticists in birth defects surveillance and epidemiology research programs: past, present and future rolesAngela E Lin, Sonja A Rasmussen, Angela Scheuerle, et al.
Neurogenetics|March 12, 2009
The impact of spermine synthase (SMS) mutations on brain morphologyShelli R Kesler, Charles Schwartz, Roger E Stevenson, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 15, 2011
Spermine synthase deficiency resulting in X-linked intellectual disability (Snyder-Robinson syndrome)Charles E Schwartz, Xaiojing Wang, Roger E Stevenson, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
X-linked intellectual disability update 2017Giovanni Neri, Charles E Schwartz, Herbert A Lubs, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 16, 2004
Neural tube defects and associated anomalies in South CarolinaRoger E Stevenson, Laurie H Seaver, Julianne S Collins, et al.
Ophthalmic Genetics|January 24, 2017
Ocular manifestations in the X-linked intellectual disability syndromesNatario L Couser, Maheer M Masood, Arthur S Aylsworth, et al.
Pageof 16