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Stephen P Robertson

Showing results (1-10 of 146) with videos related to

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European Journal of Human Genetics : EJHG|August 24, 2006
Otopalatodigital syndrome spectrum disorders: otopalatodigital syndrome types 1 and 2, frontometaphyseal dysplasia and Melnick-Needles syndromeStephen P Robertson
Current Opinion in Genetics & Development|May 27, 2005
Filamin A: phenotypic diversityStephen P Robertson
Clinical Dysmorphology|June 15, 2004
Molecular pathology of filamin A: diverse phenotypes, many functionsStephen P Robertson
Journal of Medical Ethics|April 21, 2012
Resolving the impasse on predictive genetic testing in minors: will more evidence be the solution?Stephen P Robertson, Nicola Kerruish
Novartis Foundation Symposium|November 1, 2008
Longitudinal studies of gene-environment interaction in common diseases--good value for money?Stephen P Robertson, Richie Poulton
The American Journal of Bioethics : AJOB|September 18, 2025
Structural Features of Genetic Risk and the Need for a Relational Approach to DisclosureJoey Mackle, Stephen P Robertson, Josephine Johnston
Journal of Cell Science|April 15, 2018
The filamin-B-refilin axis - spatiotemporal regulators of the actin-cytoskeleton in development and diseaseJacques Baudier, Zandra A Jenkins, Stephen P Robertson
European Journal of Human Genetics : EJHG|December 20, 2025
Robert James McKinlay ("Mac") GardnerDavid J Amor, Elsdon Storey, Stephen P Robertson
Journal of Receptor and Signal Transduction Research|March 15, 2012
TGFBR1 mutations associated with Loeys-Dietz syndrome are inactivatingSarah Cardoso, Stephen P Robertson, Philip B Daniel
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 18, 2024
Aberrant connectivity of the lateralized readiness system in non-syndromic congenital mirror movementsXueyao Lu, Elizabeth A Franz, Stephen P Robertson, et al.
Pageof 15

Showing results (1-10 of 146) with videos related to

Sort By:
Pageof 15
European Journal of Human Genetics : EJHG|August 24, 2006
Otopalatodigital syndrome spectrum disorders: otopalatodigital syndrome types 1 and 2, frontometaphyseal dysplasia and Melnick-Needles syndromeStephen P Robertson
Current Opinion in Genetics & Development|May 27, 2005
Filamin A: phenotypic diversityStephen P Robertson
Clinical Dysmorphology|June 15, 2004
Molecular pathology of filamin A: diverse phenotypes, many functionsStephen P Robertson
Journal of Medical Ethics|April 21, 2012
Resolving the impasse on predictive genetic testing in minors: will more evidence be the solution?Stephen P Robertson, Nicola Kerruish
Novartis Foundation Symposium|November 1, 2008
Longitudinal studies of gene-environment interaction in common diseases--good value for money?Stephen P Robertson, Richie Poulton
The American Journal of Bioethics : AJOB|September 18, 2025
Structural Features of Genetic Risk and the Need for a Relational Approach to DisclosureJoey Mackle, Stephen P Robertson, Josephine Johnston
Journal of Cell Science|April 15, 2018
The filamin-B-refilin axis - spatiotemporal regulators of the actin-cytoskeleton in development and diseaseJacques Baudier, Zandra A Jenkins, Stephen P Robertson
European Journal of Human Genetics : EJHG|December 20, 2025
Robert James McKinlay ("Mac") GardnerDavid J Amor, Elsdon Storey, Stephen P Robertson
Journal of Receptor and Signal Transduction Research|March 15, 2012
TGFBR1 mutations associated with Loeys-Dietz syndrome are inactivatingSarah Cardoso, Stephen P Robertson, Philip B Daniel
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 18, 2024
Aberrant connectivity of the lateralized readiness system in non-syndromic congenital mirror movementsXueyao Lu, Elizabeth A Franz, Stephen P Robertson, et al.
Pageof 15