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 Mortier

Showing results (81-90 of 95) with videos related to

Pageof 10
Sort By:
Scientific Reports|March 13, 2025
An osteobiography of a celebrity chimpanzee reflects the changing roles of modern zoosDavid M Cooper, Blessing Chidimuro, Stuart Black, et al.
The British Journal of Clinical Practice|January 1, 1988
Flurbiprofen sustained-release in OA kneeP F Boston, M F Grayson, B L Hazelman, et al.
Journal of Medical Genetics|November 25, 2003
High incidence of the R276X SALL1 mutation in sporadic but not familial Townes-Brocks syndrome and report of the first familial caseJ Kohlhase, M Liebers, J Backe, et al.
Molecular Human Reproduction|November 11, 1998
Pregnancy after preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1AA De Vos, K Sermon, H Van de Velde, et al.
Journal of Medical Genetics|July 17, 2008
Mapping of 5q35 chromosomal rearrangements within a genomically unstable regionK Buysse, A Crepel, B Menten, et al.
Journal of Medical Genetics|February 24, 2001
The mutation spectrum in Holt-Oram syndromeS J Cross, Y H Ching, Q Y Li, et al.
Human Genetics|June 1, 2000
Genotype-phenotype correlations in families with deletions in the von Hippel-Lindau (VHL) geneF Hes, R Zewald, T Peeters, et al.
Journal of Medical Genetics|November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experienceB Keren, A Hadchouel, S Saba, et al.
Human Genetics|February 11, 2003
Gene symbol: GLI3. Disease: Greig cephalopolysyndactyly syndromeS Driess, K Freese, D Bornholdt, et al.
American Journal of Human Genetics|April 16, 1998
Mutations in the EXT1 and EXT2 genes in hereditary multiple exostosesW Wuyts, W Van Hul, K De Boulle, et al.
Pageof 10

Showing results (81-90 of 95) with videos related to

Sort By:
Pageof 10
Scientific Reports|March 13, 2025
An osteobiography of a celebrity chimpanzee reflects the changing roles of modern zoosDavid M Cooper, Blessing Chidimuro, Stuart Black, et al.
The British Journal of Clinical Practice|January 1, 1988
Flurbiprofen sustained-release in OA kneeP F Boston, M F Grayson, B L Hazelman, et al.
Journal of Medical Genetics|November 25, 2003
High incidence of the R276X SALL1 mutation in sporadic but not familial Townes-Brocks syndrome and report of the first familial caseJ Kohlhase, M Liebers, J Backe, et al.
Molecular Human Reproduction|November 11, 1998
Pregnancy after preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1AA De Vos, K Sermon, H Van de Velde, et al.
Journal of Medical Genetics|July 17, 2008
Mapping of 5q35 chromosomal rearrangements within a genomically unstable regionK Buysse, A Crepel, B Menten, et al.
Journal of Medical Genetics|February 24, 2001
The mutation spectrum in Holt-Oram syndromeS J Cross, Y H Ching, Q Y Li, et al.
Human Genetics|June 1, 2000
Genotype-phenotype correlations in families with deletions in the von Hippel-Lindau (VHL) geneF Hes, R Zewald, T Peeters, et al.
Journal of Medical Genetics|November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experienceB Keren, A Hadchouel, S Saba, et al.
Human Genetics|February 11, 2003
Gene symbol: GLI3. Disease: Greig cephalopolysyndactyly syndromeS Driess, K Freese, D Bornholdt, et al.
American Journal of Human Genetics|April 16, 1998
Mutations in the EXT1 and EXT2 genes in hereditary multiple exostosesW Wuyts, W Van Hul, K De Boulle, et al.
Pageof 10