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Stephanie Wallace

Showing results (21-30 of 25) with videos related to

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ACS Sensors|August 23, 2023
Multiplexed Biosensing of Proteins and Virions with Disposable Plasmonic AssaysStephanie Wallace, Martin Kartau, Tarun Kakkar, et al.
Vaccines|January 28, 2026
Booster Immunisation with Skin-Patch-Delivered Unadjuvanted SARS-CoV-2 Spike Protein Vaccine Is Safe and Immunogenic in Healthy AdultsChristopher L D McMillan, David A Muller, Germain J P Fernando, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesityRuxandra Bachmann-Gagescu, Heather C Mefford, Charles Cowan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2019
The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathyAmélie Pinard, Stéphanie Guey, Dongchuan Guo, et al.
Human Mutation|July 17, 2015
High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype CorrelationKitiwan Rojnueangnit, Jing Xie, Alicia Gomes, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
ACS Sensors|August 23, 2023
Multiplexed Biosensing of Proteins and Virions with Disposable Plasmonic AssaysStephanie Wallace, Martin Kartau, Tarun Kakkar, et al.
Vaccines|January 28, 2026
Booster Immunisation with Skin-Patch-Delivered Unadjuvanted SARS-CoV-2 Spike Protein Vaccine Is Safe and Immunogenic in Healthy AdultsChristopher L D McMillan, David A Muller, Germain J P Fernando, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesityRuxandra Bachmann-Gagescu, Heather C Mefford, Charles Cowan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2019
The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathyAmélie Pinard, Stéphanie Guey, Dongchuan Guo, et al.
Human Mutation|July 17, 2015
High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype CorrelationKitiwan Rojnueangnit, Jing Xie, Alicia Gomes, et al.
Pageof 3