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

Ivy Jennes

Showing results (1-10 of 6) with videos related to

Pageof 1
Sort By:
The Journal of Molecular Diagnostics : JMD|January 1, 2008
Mutation screening of EXT1 and EXT2 by denaturing high-performance liquid chromatography, direct sequencing analysis, fluorescence in situ hybridization, and a new multiplex ligation-dependent probe amplification probe set in patients with multiple osteochondromasIvy Jennes, Mark M Entius, Els Van Hul, et al.
BMC Medical Genetics|June 28, 2011
Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 multiple osteochondromas familiesIvy Jennes, Danielle de Jong, Kirsten Mees, et al.
Human Mutation|February 1, 2011
Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patientsKároly Szuhai, Ivy Jennes, Danielle de Jong, et al.
Human Mutation|October 8, 2009
Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb)Ivy Jennes, Elena Pedrini, Monia Zuntini, et al.
Gene|November 1, 2011
Identification and functional characterization of the human EXT1 promoter regionIvy Jennes, Monia Zuntini, Kirsten Mees, et al.
The Journal of Bone and Joint Surgery. American Volume|January 20, 2012
Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of "protective" and "risk" factorsElena Pedrini, Ivy Jennes, Morena Tremosini, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
The Journal of Molecular Diagnostics : JMD|January 1, 2008
Mutation screening of EXT1 and EXT2 by denaturing high-performance liquid chromatography, direct sequencing analysis, fluorescence in situ hybridization, and a new multiplex ligation-dependent probe amplification probe set in patients with multiple osteochondromasIvy Jennes, Mark M Entius, Els Van Hul, et al.
BMC Medical Genetics|June 28, 2011
Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 multiple osteochondromas familiesIvy Jennes, Danielle de Jong, Kirsten Mees, et al.
Human Mutation|February 1, 2011
Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patientsKároly Szuhai, Ivy Jennes, Danielle de Jong, et al.
Human Mutation|October 8, 2009
Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb)Ivy Jennes, Elena Pedrini, Monia Zuntini, et al.
Gene|November 1, 2011
Identification and functional characterization of the human EXT1 promoter regionIvy Jennes, Monia Zuntini, Kirsten Mees, et al.
The Journal of Bone and Joint Surgery. American Volume|January 20, 2012
Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of "protective" and "risk" factorsElena Pedrini, Ivy Jennes, Morena Tremosini, et al.
Pageof 1