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

N Sakati

Showing results (31-40 of 36) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 36 results.
Annals of Saudi Medicine|July 1, 1994
Glutaric aciduria yype 1: First reported cases in three Saudi patientsR Coates, M Rashed, Z Rahbeeni, et al.
American Journal of Medical Genetics. Part A|July 31, 2014
Marshall syndrome: further evidence of a distinct phenotypic entity and report of new findingsO Khalifa, F Imtiaz, K Ramzan, et al.
Brain & Development|November 1, 1994
Ethylmalonic aciduria: an organic acidemia with CNS involvement and vasculopathyP T Ozand, M Rashed, D S Millington, et al.
Clinical Genetics|August 18, 1999
Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiencyE Al-Jishi, B F Meyer, M S Rashed, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 1998
Four contiguous amino acid substitutions, identified in patients with Laron syndrome, differently affect the binding affinity and intracellular trafficking of the growth hormone receptorJ Wojcik, M A Berg, N Esposito, et al.
Clinical Genetics|June 24, 2011
Smith-Lemli-Opitz syndrome among ArabsM Al-Owain, F Imtiaz, T Shuaib, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Annals of Saudi Medicine|July 1, 1994
Glutaric aciduria yype 1: First reported cases in three Saudi patientsR Coates, M Rashed, Z Rahbeeni, et al.
American Journal of Medical Genetics. Part A|July 31, 2014
Marshall syndrome: further evidence of a distinct phenotypic entity and report of new findingsO Khalifa, F Imtiaz, K Ramzan, et al.
Brain & Development|November 1, 1994
Ethylmalonic aciduria: an organic acidemia with CNS involvement and vasculopathyP T Ozand, M Rashed, D S Millington, et al.
Clinical Genetics|August 18, 1999
Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiencyE Al-Jishi, B F Meyer, M S Rashed, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 1998
Four contiguous amino acid substitutions, identified in patients with Laron syndrome, differently affect the binding affinity and intracellular trafficking of the growth hormone receptorJ Wojcik, M A Berg, N Esposito, et al.
Clinical Genetics|June 24, 2011
Smith-Lemli-Opitz syndrome among ArabsM Al-Owain, F Imtiaz, T Shuaib, et al.
Pageof 4