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

Benjamin Glick

Showing results (1-10 of 6) with videos related to

Pageof 1
Sort By:
Molecular Biology of the Cell|March 17, 2011
Organelle structure and biogenesisMaya Schuldiner, Benjamin Glick
Clinical Pediatrics|June 2, 2009
Does picky eating affect weight-for-length measurements in young children?Sivan Ekstein, David Laniado, Benjamin Glick
Journal of Child Neurology|June 2, 2011
Down syndrome and attention-deficit/hyperactivity disorder (ADHD)Sivan Ekstein, Benjamin Glick, Michal Weill, et al.
Journal of Child Neurology|July 21, 2007
Congenital myopathies in Israeli familiesKarin Weiss, Yehuda Shapira, Benjamin Glick, et al.
Human Molecular Genetics|June 23, 2009
Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposisRuben Attali, Nasim Warwar, Ariel Israel, et al.
Brain : a Journal of Neurology|July 17, 2015
Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorderAlexander Lossos, Nimrod Elazar, Israela Lerer, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Molecular Biology of the Cell|March 17, 2011
Organelle structure and biogenesisMaya Schuldiner, Benjamin Glick
Clinical Pediatrics|June 2, 2009
Does picky eating affect weight-for-length measurements in young children?Sivan Ekstein, David Laniado, Benjamin Glick
Journal of Child Neurology|June 2, 2011
Down syndrome and attention-deficit/hyperactivity disorder (ADHD)Sivan Ekstein, Benjamin Glick, Michal Weill, et al.
Journal of Child Neurology|July 21, 2007
Congenital myopathies in Israeli familiesKarin Weiss, Yehuda Shapira, Benjamin Glick, et al.
Human Molecular Genetics|June 23, 2009
Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposisRuben Attali, Nasim Warwar, Ariel Israel, et al.
Brain : a Journal of Neurology|July 17, 2015
Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorderAlexander Lossos, Nimrod Elazar, Israela Lerer, et al.
Pageof 1