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

S LeBlond

Showing results (11-20 of 72) with videos related to

Pageof 8
Sort By:
Parkinsonism & Related Disorders|May 13, 2015
LRRK2 mutations in Parkinson disease; a sex effect or lack thereof? A meta-analysisZiv Gan-Or, Claire S Leblond, Victoria Mallett, et al.
Behavioural Brain Research|September 3, 2013
The Autism ProSAP1/Shank2 mouse model displays quantitative and structural abnormalities in ultrasonic vocalisationsElodie Ey, Nicolas Torquet, Anne-Marie Le Sourd, et al.
Neurology. Genetics|April 29, 2016
De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopiaClaire S Leblond, Alina Webber, Ziv Gan-Or, et al.
Molecular and Cellular Neurosciences|May 1, 2021
Operative list of genes associated with autism and neurodevelopmental disorders based on database reviewClaire S Leblond, Thuy-Linh Le, Simon Malesys, et al.
Genomics|March 1, 1991
Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophyG Shutler, A E MacKenzie, H Brunner, et al.
Neurology. Genetics|May 2, 2019
Somatic expansion of the <i>C9orf72</i> hexanucleotide repeat does not occur in ALS spinal cord tissuesJay P Ross, Claire S Leblond, Hélène Catoire, et al.
The Science of the Total Environment|October 16, 2012
An inventory of trace elements inputs to French agricultural soilsE Belon, M Boisson, I Z Deportes, et al.
American Journal of Human Genetics|November 1, 1991
D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19qC Tsilfidis, A E MacKenzie, G Shutler, et al.
American Journal of Human Genetics|June 1, 1990
The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophyA E MacKenzie, R G Korneluk, F Zorzato, et al.
Scientific Reports|December 20, 2017
Heritability of the melatonin synthesis variability in autism spectrum disordersMarion Benabou, Thomas Rolland, Claire S Leblond, et al.
Pageof 8

Showing results (11-20 of 72) with videos related to

Sort By:
Pageof 8
Parkinsonism & Related Disorders|May 13, 2015
LRRK2 mutations in Parkinson disease; a sex effect or lack thereof? A meta-analysisZiv Gan-Or, Claire S Leblond, Victoria Mallett, et al.
Behavioural Brain Research|September 3, 2013
The Autism ProSAP1/Shank2 mouse model displays quantitative and structural abnormalities in ultrasonic vocalisationsElodie Ey, Nicolas Torquet, Anne-Marie Le Sourd, et al.
Neurology. Genetics|April 29, 2016
De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopiaClaire S Leblond, Alina Webber, Ziv Gan-Or, et al.
Molecular and Cellular Neurosciences|May 1, 2021
Operative list of genes associated with autism and neurodevelopmental disorders based on database reviewClaire S Leblond, Thuy-Linh Le, Simon Malesys, et al.
Genomics|March 1, 1991
Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophyG Shutler, A E MacKenzie, H Brunner, et al.
Neurology. Genetics|May 2, 2019
Somatic expansion of the <i>C9orf72</i> hexanucleotide repeat does not occur in ALS spinal cord tissuesJay P Ross, Claire S Leblond, Hélène Catoire, et al.
The Science of the Total Environment|October 16, 2012
An inventory of trace elements inputs to French agricultural soilsE Belon, M Boisson, I Z Deportes, et al.
American Journal of Human Genetics|November 1, 1991
D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19qC Tsilfidis, A E MacKenzie, G Shutler, et al.
American Journal of Human Genetics|June 1, 1990
The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophyA E MacKenzie, R G Korneluk, F Zorzato, et al.
Scientific Reports|December 20, 2017
Heritability of the melatonin synthesis variability in autism spectrum disordersMarion Benabou, Thomas Rolland, Claire S Leblond, et al.
Pageof 8