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

U Felbor

Showing results (21-30 of 24) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 24 results.
European Journal of Human Genetics : EJHG|September 14, 1999
Allelic heterogeneity of alkaptonuria in Central EuropeC R Müller, A Fregin, S Srsen, et al.
Hamostaseologie|November 6, 2015
Large deletions play a minor but essential role in congenital coagulation factor VII and X deficienciesM Rath, J Najm, H Sirb, et al.
American Journal of Human Genetics|May 23, 2001
A nonsense mutation in MSX1 causes Witkop syndromeD Jumlongras, M Bei, J M Stimson, et al.
Trials|June 2, 2025
dVP_FAM-development and evaluation of a transsectoral digital care platform for individuals with familial cancer risks: study protocol for a multi-centre, cluster-randomised, mixed-methods studyK Klein, F Kendel, S Schüürhuis, et al.
Pageof 3

Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
European Journal of Human Genetics : EJHG|September 14, 1999
Allelic heterogeneity of alkaptonuria in Central EuropeC R Müller, A Fregin, S Srsen, et al.
Hamostaseologie|November 6, 2015
Large deletions play a minor but essential role in congenital coagulation factor VII and X deficienciesM Rath, J Najm, H Sirb, et al.
American Journal of Human Genetics|May 23, 2001
A nonsense mutation in MSX1 causes Witkop syndromeD Jumlongras, M Bei, J M Stimson, et al.
Trials|June 2, 2025
dVP_FAM-development and evaluation of a transsectoral digital care platform for individuals with familial cancer risks: study protocol for a multi-centre, cluster-randomised, mixed-methods studyK Klein, F Kendel, S Schüürhuis, et al.
Pageof 3