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

Richard Redon

Showing results (51-60 of 131) with videos related to

Pageof 14
Sort By:
Genome Research|September 9, 2008
Copy number variation and evolution in humans and chimpanzeesGeorge H Perry, Fengtang Yang, Tomas Marques-Bonet, et al.
Stem Cell Research|January 9, 2022
Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic backgroundAurore Girardeau, Diane Atticus, Robin Canac, et al.
American Journal of Human Genetics|July 7, 2010
Mesomelia-synostoses syndrome results from deletion of SULF1 and SLCO5A1 genes at 8q13Bertrand Isidor, Olivier Pichon, Richard Redon, et al.
European Journal of Human Genetics : EJHG|October 9, 2019
Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene clusterCédric Le Caignec, Olivier Pichon, Annaig Briand, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 24, 2020
Location of intracranial aneurysms is the main factor associated with rupture in the ICAN populationOlivia Rousseau, Matilde Karakachoff, Alban Gaignard, et al.
Annals of Neurology|January 26, 2018
A novel mutation in the transmembrane 6 domain of GABBR2 leads to a Rett-like phenotypeMarie-Laure Vuillaume, Médéric Jeanne, Li Xue, et al.
Biochemical Society Transactions|March 20, 2010
Confirmed rare copy number variants implicate novel genes in schizophreniaGloria W C Tam, Louie N van de Lagemaat, Richard Redon, et al.
Neurosurgery|April 1, 2017
Understanding the Pathophysiology of Intracranial Aneurysm: The ICAN ProjectRomain Bourcier, Stéphanie Chatel, Emmanuelle Bourcereau, et al.
Science (New York, N.Y.)|February 10, 2007
Relative impact of nucleotide and copy number variation on gene expression phenotypesBarbara E Stranger, Matthew S Forrest, Mark Dunning, et al.
Circulation. Cardiovascular Genetics|December 9, 2015
Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the AortaMarta Sanchez-Castro, Hadja Eldjouzi, Eric Charpentier, et al.
Pageof 14

Showing results (51-60 of 131) with videos related to

Sort By:
Pageof 14
Genome Research|September 9, 2008
Copy number variation and evolution in humans and chimpanzeesGeorge H Perry, Fengtang Yang, Tomas Marques-Bonet, et al.
Stem Cell Research|January 9, 2022
Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic backgroundAurore Girardeau, Diane Atticus, Robin Canac, et al.
American Journal of Human Genetics|July 7, 2010
Mesomelia-synostoses syndrome results from deletion of SULF1 and SLCO5A1 genes at 8q13Bertrand Isidor, Olivier Pichon, Richard Redon, et al.
European Journal of Human Genetics : EJHG|October 9, 2019
Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene clusterCédric Le Caignec, Olivier Pichon, Annaig Briand, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 24, 2020
Location of intracranial aneurysms is the main factor associated with rupture in the ICAN populationOlivia Rousseau, Matilde Karakachoff, Alban Gaignard, et al.
Annals of Neurology|January 26, 2018
A novel mutation in the transmembrane 6 domain of GABBR2 leads to a Rett-like phenotypeMarie-Laure Vuillaume, Médéric Jeanne, Li Xue, et al.
Biochemical Society Transactions|March 20, 2010
Confirmed rare copy number variants implicate novel genes in schizophreniaGloria W C Tam, Louie N van de Lagemaat, Richard Redon, et al.
Neurosurgery|April 1, 2017
Understanding the Pathophysiology of Intracranial Aneurysm: The ICAN ProjectRomain Bourcier, Stéphanie Chatel, Emmanuelle Bourcereau, et al.
Science (New York, N.Y.)|February 10, 2007
Relative impact of nucleotide and copy number variation on gene expression phenotypesBarbara E Stranger, Matthew S Forrest, Mark Dunning, et al.
Circulation. Cardiovascular Genetics|December 9, 2015
Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the AortaMarta Sanchez-Castro, Hadja Eldjouzi, Eric Charpentier, et al.
Pageof 14