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

M Hendrickx

Showing results (121-130 of 126) with videos related to

Pageof 13
Sort By:
You have reached the last page of results.This site can display upto 126 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patientsRudy G E van Eijsden, Mike Gerards, Lars M T Eijssen, et al.
Journal of Medical Genetics|June 23, 2009
Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndromeM Gerards, W Sluiter, B J C van den Bosch, et al.
JIMD Reports|March 4, 2015
Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial MyopathyI M L W Körver-Keularts, M de Visser, H D Bakker, et al.
The Journal of Pediatrics|January 14, 2017
Rapid Resolution of Blended or Composite Multigenic Disease in Infants by Whole-Exome SequencingTom E J Theunissen, Suzanne C E H Sallevelt, Debby M E I Hellebrekers, et al.
Bioinformatics (Oxford, England)|December 16, 2014
diXa: a data infrastructure for chemical safety assessmentDiana M Hendrickx, Hugo J W L Aerts, Florian Caiment, et al.
Aerobiologia|June 6, 2017
Spatial and temporal variations in airborne <i>Ambrosia</i> pollen in EuropeB Sikoparija, C A Skjøth, S Celenk, et al.
Pageof 13

Showing results (121-130 of 126) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 126 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patientsRudy G E van Eijsden, Mike Gerards, Lars M T Eijssen, et al.
Journal of Medical Genetics|June 23, 2009
Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndromeM Gerards, W Sluiter, B J C van den Bosch, et al.
JIMD Reports|March 4, 2015
Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial MyopathyI M L W Körver-Keularts, M de Visser, H D Bakker, et al.
The Journal of Pediatrics|January 14, 2017
Rapid Resolution of Blended or Composite Multigenic Disease in Infants by Whole-Exome SequencingTom E J Theunissen, Suzanne C E H Sallevelt, Debby M E I Hellebrekers, et al.
Bioinformatics (Oxford, England)|December 16, 2014
diXa: a data infrastructure for chemical safety assessmentDiana M Hendrickx, Hugo J W L Aerts, Florian Caiment, et al.
Aerobiologia|June 6, 2017
Spatial and temporal variations in airborne <i>Ambrosia</i> pollen in EuropeB Sikoparija, C A Skjøth, S Celenk, et al.
Pageof 13