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

V Adir

Showing results (1-10 of 4) with videos related to

Pageof 1
Sort By:
The Journal of Clinical Investigation|August 1, 1994
LAP (NF-IL6) transactivates the collagen alpha 1(I) gene from a 5' regulatory regionK Houglum, M Buck, V Adir, et al.
Journal of Medical Genetics|May 4, 2004
Spondylo-epi-metaphyseal dysplasia (SEMD) matrilin 3 type: homozygote matrilin 3 mutation in a novel form of SEMDZ U Borochowitz, D Scheffer, V Adir, et al.
Parkinsonism & Related Disorders|August 31, 2015
SMPD1 mutations and Parkinson diseaseE Dagan, V Adir, I Schlesinger, et al.
Clinical Dysmorphology|September 14, 2020
A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1Amir Peleg, Alina Kurolap, Lena Sagi-Dain, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
The Journal of Clinical Investigation|August 1, 1994
LAP (NF-IL6) transactivates the collagen alpha 1(I) gene from a 5' regulatory regionK Houglum, M Buck, V Adir, et al.
Journal of Medical Genetics|May 4, 2004
Spondylo-epi-metaphyseal dysplasia (SEMD) matrilin 3 type: homozygote matrilin 3 mutation in a novel form of SEMDZ U Borochowitz, D Scheffer, V Adir, et al.
Parkinsonism & Related Disorders|August 31, 2015
SMPD1 mutations and Parkinson diseaseE Dagan, V Adir, I Schlesinger, et al.
Clinical Dysmorphology|September 14, 2020
A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1Amir Peleg, Alina Kurolap, Lena Sagi-Dain, et al.
Pageof 1