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Dominique Martin

Showing results (31-40 of 77) with videos related to

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Systematic Reviews|September 9, 2021
Protocol for a systematic review of outcomes from microsurgical free-tissue transfer performed on short-term collaborative surgical trips in low-income and middle-income countriesHenry T de Berker, Urška Čebron, Daniel Bradley, et al.
Plastic and Reconstructive Surgery|March 26, 2019
Twenty-Five Years of Experience with the Submental Flap in Facial Reconstruction: Evolution and Technical Refinements following 311 Cases in Europe and AfricaBaptiste Bertrand, Calum Sinclair Honeyman, Angel Emparanza, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2023
Late-life shift in caloric intake affects fly metabolism and longevityMichael Li, Jacob Macro, Kali Meadows, et al.
The Journal of Clinical Endocrinology and Metabolism|June 18, 2009
Familial frameshift SRY mutation inherited from a mosaic father with testicular dysgenesis syndromeBertrand Isidor, Carmen Capito, Françoise Paris, et al.
Birth Defects Research|January 10, 2018
Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1Séverine Bacrot, Charlotte Mechler, Naima Talhi, et al.
American Journal of Human Genetics|August 30, 2016
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex FamiliesVirpi M Leppa, Stephanie N Kravitz, Christa Lese Martin, et al.
European Journal of Medical Genetics|December 23, 2015
Karyotype is not dead (yet)!Laurent Pasquier, Mélanie Fradin, Elouan Chérot, et al.
Journal of Critical Care|July 17, 2020
Conflicts of interest in the context of end of life care for potential organ donors in AustraliaFrank M P van Haren, Angus Carter, Elena Cavazzoni, et al.
European Journal of Human Genetics : EJHG|November 22, 2012
Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomasBertrand Isidor, Franck Bourdeaut, Delfine Lafon, et al.
Human Mutation|October 6, 2009
Missense mutations of conserved glycine residues in fibrillin-1 highlight a potential subtype of cb-EGF-like domainsPhilippe Khau Van Kien, David Baux, Nathalie Pallares-Ruiz, et al.
Pageof 8

Showing results (31-40 of 77) with videos related to

Sort By:
Pageof 8
Systematic Reviews|September 9, 2021
Protocol for a systematic review of outcomes from microsurgical free-tissue transfer performed on short-term collaborative surgical trips in low-income and middle-income countriesHenry T de Berker, Urška Čebron, Daniel Bradley, et al.
Plastic and Reconstructive Surgery|March 26, 2019
Twenty-Five Years of Experience with the Submental Flap in Facial Reconstruction: Evolution and Technical Refinements following 311 Cases in Europe and AfricaBaptiste Bertrand, Calum Sinclair Honeyman, Angel Emparanza, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2023
Late-life shift in caloric intake affects fly metabolism and longevityMichael Li, Jacob Macro, Kali Meadows, et al.
The Journal of Clinical Endocrinology and Metabolism|June 18, 2009
Familial frameshift SRY mutation inherited from a mosaic father with testicular dysgenesis syndromeBertrand Isidor, Carmen Capito, Françoise Paris, et al.
Birth Defects Research|January 10, 2018
Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1Séverine Bacrot, Charlotte Mechler, Naima Talhi, et al.
American Journal of Human Genetics|August 30, 2016
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex FamiliesVirpi M Leppa, Stephanie N Kravitz, Christa Lese Martin, et al.
European Journal of Medical Genetics|December 23, 2015
Karyotype is not dead (yet)!Laurent Pasquier, Mélanie Fradin, Elouan Chérot, et al.
Journal of Critical Care|July 17, 2020
Conflicts of interest in the context of end of life care for potential organ donors in AustraliaFrank M P van Haren, Angus Carter, Elena Cavazzoni, et al.
European Journal of Human Genetics : EJHG|November 22, 2012
Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomasBertrand Isidor, Franck Bourdeaut, Delfine Lafon, et al.
Human Mutation|October 6, 2009
Missense mutations of conserved glycine residues in fibrillin-1 highlight a potential subtype of cb-EGF-like domainsPhilippe Khau Van Kien, David Baux, Nathalie Pallares-Ruiz, et al.
Pageof 8