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

J Bonaventure

Showing results (31-40 of 81) with videos related to

Pageof 9
Sort By:
Human Genetics|September 1, 1992
Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant geneJ Bonaventure, C Philippe, G Plessis, et al.
American Journal of Medical Genetics|May 3, 1996
Common mutations in the fibroblast growth factor receptor 3 (FGFR 3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfismJ Bonaventure, F Rousseau, L Legeai-Mallet, et al.
Pathologie-Biologie|February 10, 2009
Bypassing melanocyte senescence by beta-catenin: a novel way to promote melanomaL Larue, F Luciani, M Kumasaka, et al.
Bone|January 1, 1991
Morphological and biochemical studies of a mouse mutant (fro/fro) with bone fragilityM P Muriel, J Bonaventure, R Stanescu, et al.
The Histochemical Journal|September 1, 1994
Localization of the expression of type I, II and III collagen genes in human normal and hypochondrogenesis cartilage canalsD Le Guellec, F Mallein-Gerin, I Treilleux, et al.
Journal of Medical Genetics|February 9, 1999
Sex related expressivity of the phenotype in coronal craniosynostosis caused by the recurrent P250R FGFR3 mutationE Lajeunie, V El Ghouzzi, M Le Merrer, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|October 1, 1996
Common mutations in the gene encoding fibroblast growth factor receptor 3 account for achondroplasia, hypochondroplasia and thanatophoric dysplasiaJ Bonaventure, F Rousseau, L Legeai-Mallet, et al.
Nature Genetics|February 1, 1995
FGFR2 mutations in Pfeiffer syndromeE Lajeunie, H W Ma, J Bonaventure, et al.
American Journal of Medical Genetics|July 1, 1989
A new lethal brittle bone syndrome with increased amount of type V collagen in a patientJ Bonaventure, L Zylberberg, L Cohen-Solal, et al.
Journal of Medical Genetics|July 4, 2001
Genotype-phenotype correlation in hereditary multiple exostosesC Francannet, A Cohen-Tanugi, M Le Merrer, et al.
Pageof 9

Showing results (31-40 of 81) with videos related to

Sort By:
Pageof 9
Human Genetics|September 1, 1992
Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant geneJ Bonaventure, C Philippe, G Plessis, et al.
American Journal of Medical Genetics|May 3, 1996
Common mutations in the fibroblast growth factor receptor 3 (FGFR 3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfismJ Bonaventure, F Rousseau, L Legeai-Mallet, et al.
Pathologie-Biologie|February 10, 2009
Bypassing melanocyte senescence by beta-catenin: a novel way to promote melanomaL Larue, F Luciani, M Kumasaka, et al.
Bone|January 1, 1991
Morphological and biochemical studies of a mouse mutant (fro/fro) with bone fragilityM P Muriel, J Bonaventure, R Stanescu, et al.
The Histochemical Journal|September 1, 1994
Localization of the expression of type I, II and III collagen genes in human normal and hypochondrogenesis cartilage canalsD Le Guellec, F Mallein-Gerin, I Treilleux, et al.
Journal of Medical Genetics|February 9, 1999
Sex related expressivity of the phenotype in coronal craniosynostosis caused by the recurrent P250R FGFR3 mutationE Lajeunie, V El Ghouzzi, M Le Merrer, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|October 1, 1996
Common mutations in the gene encoding fibroblast growth factor receptor 3 account for achondroplasia, hypochondroplasia and thanatophoric dysplasiaJ Bonaventure, F Rousseau, L Legeai-Mallet, et al.
Nature Genetics|February 1, 1995
FGFR2 mutations in Pfeiffer syndromeE Lajeunie, H W Ma, J Bonaventure, et al.
American Journal of Medical Genetics|July 1, 1989
A new lethal brittle bone syndrome with increased amount of type V collagen in a patientJ Bonaventure, L Zylberberg, L Cohen-Solal, et al.
Journal of Medical Genetics|July 4, 2001
Genotype-phenotype correlation in hereditary multiple exostosesC Francannet, A Cohen-Tanugi, M Le Merrer, et al.
Pageof 9