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

G Asteggiano

Showing results (11-20 of 14) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 14 results.
Scientific Reports|September 19, 2014
A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDGM A Delgado, G Martinez-Domenech, P Sarrión, et al.
Archivos Argentinos De Pediatria|March 3, 2015
[Double mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses]Francisco Cammarata-Scalisi, Mónica Cozar, Daniel Grinberg, et al.
Scientific Reports|February 27, 2013
Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromasP Sarrión, A Sangorrin, R Urreizti, et al.
Plos Genetics|December 19, 2013
MAN1B1 deficiency: an unexpected CDG-IIDaisy Rymen, Romain Peanne, María B Millón, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Scientific Reports|September 19, 2014
A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDGM A Delgado, G Martinez-Domenech, P Sarrión, et al.
Archivos Argentinos De Pediatria|March 3, 2015
[Double mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses]Francisco Cammarata-Scalisi, Mónica Cozar, Daniel Grinberg, et al.
Scientific Reports|February 27, 2013
Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromasP Sarrión, A Sangorrin, R Urreizti, et al.
Plos Genetics|December 19, 2013
MAN1B1 deficiency: an unexpected CDG-IIDaisy Rymen, Romain Peanne, María B Millón, et al.
Pageof 2