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

L Guion

Showing results (51-60 of 55) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 55 results.
American Journal of Medical Genetics. Part A|May 31, 2017
Mandibulofacial dysostosis Bauru type: Refining the phenotypePriscila P Moura, Nancy M Kokitsu-Nakata, Marília S Yatabe, et al.
Bone|August 17, 2021
A novel intronic variant in PIGB in Acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defectsEleonora Palagano, Christopher T Gordon, Paolo Uva, et al.
Nature Genetics|December 1, 1995
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2N H Robin, G J Feldman, A L Aronson, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndromeVanessa L Romanelli Tavares, Roseli M Zechi-Ceide, Debora R Bertola, et al.
European Journal of Human Genetics : EJHG|July 17, 2014
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effectVanessa L Romanelli Tavares, Christopher T Gordon, Roseli M Zechi-Ceide, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
American Journal of Medical Genetics. Part A|May 31, 2017
Mandibulofacial dysostosis Bauru type: Refining the phenotypePriscila P Moura, Nancy M Kokitsu-Nakata, Marília S Yatabe, et al.
Bone|August 17, 2021
A novel intronic variant in PIGB in Acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defectsEleonora Palagano, Christopher T Gordon, Paolo Uva, et al.
Nature Genetics|December 1, 1995
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2N H Robin, G J Feldman, A L Aronson, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndromeVanessa L Romanelli Tavares, Roseli M Zechi-Ceide, Debora R Bertola, et al.
European Journal of Human Genetics : EJHG|July 17, 2014
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effectVanessa L Romanelli Tavares, Christopher T Gordon, Roseli M Zechi-Ceide, et al.
Pageof 6