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

Caroline Robberecht

Showing results (11-20 of 14) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 14 results.
Inflammatory Bowel Diseases|November 24, 2015
Genome-Wide Copy Number Variation Scan Identifies Complement Component C4 as Novel Susceptibility Gene for Crohn's DiseaseIsabelle Cleynen, Peter Konings, Caroline Robberecht, et al.
Acta Neuropathologica Communications|November 12, 2015
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brainsJonathan Janssens, Stéphanie Philtjens, Gernot Kleinberger, et al.
American Journal of Human Genetics|August 5, 2014
Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disordersIan M Campbell, Bo Yuan, Caroline Robberecht, et al.
Neurobiology of Aging|March 23, 2015
Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium studyElise Cuyvers, Julie van der Zee, Karolien Bettens, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Inflammatory Bowel Diseases|November 24, 2015
Genome-Wide Copy Number Variation Scan Identifies Complement Component C4 as Novel Susceptibility Gene for Crohn's DiseaseIsabelle Cleynen, Peter Konings, Caroline Robberecht, et al.
Acta Neuropathologica Communications|November 12, 2015
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brainsJonathan Janssens, Stéphanie Philtjens, Gernot Kleinberger, et al.
American Journal of Human Genetics|August 5, 2014
Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disordersIan M Campbell, Bo Yuan, Caroline Robberecht, et al.
Neurobiology of Aging|March 23, 2015
Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium studyElise Cuyvers, Julie van der Zee, Karolien Bettens, et al.
Pageof 2