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Susan Winter

Showing results (1-10 of 15) with videos related to

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Annals of Nutrition & Metabolism|December 9, 2016
ForewordSusan Winter
Science and Engineering Ethics|July 3, 2020
Role-Playing Computer Ethics: Designing and Evaluating the Privacy by Design (PbD) SimulationKatie Shilton, Donal Heidenblad, Adam Porter, et al.
Critical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine|March 4, 2010
Particulate face masks for protection against airborne pathogens - one size does not fit all: an observational studySusan Winter, Jane H Thomas, Dianne P Stephens, et al.
Journal of Clinical and Translational Science|June 27, 2017
Organizational and training factors that promote team science: A qualitative analysis and application of theory to the National Institutes of Health's BIRCWH career development programJeanne-Marie Guise, Susan Winter, Stephen M Fiore, et al.
Annals of Nutrition & Metabolism|December 9, 2016
Round Table DiscussionSusan Winter, Neil R M Buist, Nicola Longo, et al.
Journal of Medical Genetics|November 28, 2018
Biallelic disruption of <i>PKDCC</i> is associated with a skeletal disorder characterised by rhizomelic shortening of extremities and dysmorphic featuresSamin A Sajan, Jaya Ganesh, Deepali N Shinde, et al.
European Journal of Human Genetics : EJHG|August 9, 2012
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disordersSandesh C S Nagamani, Ayelet Erez, Bruria Ben-Zeev, et al.
Clinical Therapeutics|September 9, 2025
The Chilling of Data Sharing and Reuse: Lives at Greater Risk in the Current EraJoel Cutcher-Gershenfeld, Paul Beninger, Alan Blatecky, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
The role of IQSEC2 in syndromic intellectual disability: Narrowing the diagnostic odysseyBenjamin M Helm, Zoe Powis, Carlos E Prada, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic featuresGanka Douglas, Megan T Cho, Aida Telegrafi, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Annals of Nutrition & Metabolism|December 9, 2016
ForewordSusan Winter
Science and Engineering Ethics|July 3, 2020
Role-Playing Computer Ethics: Designing and Evaluating the Privacy by Design (PbD) SimulationKatie Shilton, Donal Heidenblad, Adam Porter, et al.
Critical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine|March 4, 2010
Particulate face masks for protection against airborne pathogens - one size does not fit all: an observational studySusan Winter, Jane H Thomas, Dianne P Stephens, et al.
Journal of Clinical and Translational Science|June 27, 2017
Organizational and training factors that promote team science: A qualitative analysis and application of theory to the National Institutes of Health's BIRCWH career development programJeanne-Marie Guise, Susan Winter, Stephen M Fiore, et al.
Annals of Nutrition & Metabolism|December 9, 2016
Round Table DiscussionSusan Winter, Neil R M Buist, Nicola Longo, et al.
Journal of Medical Genetics|November 28, 2018
Biallelic disruption of <i>PKDCC</i> is associated with a skeletal disorder characterised by rhizomelic shortening of extremities and dysmorphic featuresSamin A Sajan, Jaya Ganesh, Deepali N Shinde, et al.
European Journal of Human Genetics : EJHG|August 9, 2012
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disordersSandesh C S Nagamani, Ayelet Erez, Bruria Ben-Zeev, et al.
Clinical Therapeutics|September 9, 2025
The Chilling of Data Sharing and Reuse: Lives at Greater Risk in the Current EraJoel Cutcher-Gershenfeld, Paul Beninger, Alan Blatecky, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
The role of IQSEC2 in syndromic intellectual disability: Narrowing the diagnostic odysseyBenjamin M Helm, Zoe Powis, Carlos E Prada, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic featuresGanka Douglas, Megan T Cho, Aida Telegrafi, et al.
Pageof 2