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

O F Brouwer

Showing results (111-120 of 114) with videos related to

Pageof 12
Sort By:
You have reached the last page of results.This site can display upto 114 results.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 6, 2013
Impact of introduction of mid-trimester scan on pregnancy outcome of open spina bifida in The NetherlandsJ H Fleurke-Rozema, T A Vogel, B J Voskamp, et al.
Neurogenetics|July 3, 2017
Male patients affected by mosaic PCDH19 mutations: five new casesI M de Lange, P Rump, R F Neuteboom, et al.
Pediatrics|April 1, 1997
The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patientsK M Gibson, E Christensen, C Jakobs, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 5, 2019
A clinical diagnostic algorithm for early onset cerebellar ataxiaR Brandsma, C C Verschuuren-Bemelmans, D Amrom, et al.
Pageof 12

Showing results (111-120 of 114) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 114 results.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 6, 2013
Impact of introduction of mid-trimester scan on pregnancy outcome of open spina bifida in The NetherlandsJ H Fleurke-Rozema, T A Vogel, B J Voskamp, et al.
Neurogenetics|July 3, 2017
Male patients affected by mosaic PCDH19 mutations: five new casesI M de Lange, P Rump, R F Neuteboom, et al.
Pediatrics|April 1, 1997
The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patientsK M Gibson, E Christensen, C Jakobs, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 5, 2019
A clinical diagnostic algorithm for early onset cerebellar ataxiaR Brandsma, C C Verschuuren-Bemelmans, D Amrom, et al.
Pageof 12