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

Carla Lintas

Showing results (51-60 of 53) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 53 results.
Molecular Genetics & Genomic Medicine|June 27, 2020
FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex familyFrancesca Cucinotta, Arianna Ricciardello, Laura Turriziani, et al.
Lung Cancer (Amsterdam, Netherlands)|March 1, 2026
Family history enrichment in Non-Small cell Lung Cancer: A cross-sectional - prospective study to inform referral for germline testingFabrizio Citarella, Francesco M Venanzi, Giulia Di Giovanni, et al.
Nature Genetics|August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autismJack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Pageof 6

Showing results (51-60 of 53) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 53 results.
Molecular Genetics & Genomic Medicine|June 27, 2020
FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex familyFrancesca Cucinotta, Arianna Ricciardello, Laura Turriziani, et al.
Lung Cancer (Amsterdam, Netherlands)|March 1, 2026
Family history enrichment in Non-Small cell Lung Cancer: A cross-sectional - prospective study to inform referral for germline testingFabrizio Citarella, Francesco M Venanzi, Giulia Di Giovanni, et al.
Nature Genetics|August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autismJack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Pageof 6