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Showing results (941-950 of 951) with videos related to

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Human Mutation|March 3, 2016
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported PatientsBobby G Ng, Sergey A Shiryaev, Daisy Rymen, et al.
Genome Medicine|October 25, 2025
Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromesYingxi Wang, Eleanor I Sams, Rachel Slaugh, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2025
Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p SyndromesYingxi Wang, Eleanor I Sams, Rachel Slaugh, et al.
Science (New York, N.Y.)|May 26, 2009
Antigenic and genetic characteristics of swine-origin 2009 A(H1N1) influenza viruses circulating in humansRebecca J Garten, C Todd Davis, Colin A Russell, et al.
Science Translational Medicine|May 31, 2023
PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon productionFrédéric Ebstein, Sébastien Küry, Victoria Most, et al.
Human Mutation|March 19, 2013
Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domainPartha Sen, Yaping Yang, Colby Navarro, et al.
JAMA Pediatrics|February 28, 2017
Families as Partners in Hospital Error and Adverse Event SurveillanceAlisa Khan, Maitreya Coffey, Katherine P Litterer, et al.
Nature Methods|February 9, 2026
Addressing pandemic-wide systematic errors in the SARS-CoV-2 phylogenyMartin Hunt, Angie S Hinrichs, Daniel Anderson, et al.
Biorxiv : the Preprint Server for Biology|May 15, 2024
Addressing pandemic-wide systematic errors in the SARS-CoV-2 phylogenyMartin Hunt, Angie S Hinrichs, Daniel Anderson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Pageof 96

Showing results (941-950 of 951) with videos related to

Sort By:
Pageof 96
Human Mutation|March 3, 2016
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported PatientsBobby G Ng, Sergey A Shiryaev, Daisy Rymen, et al.
Genome Medicine|October 25, 2025
Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromesYingxi Wang, Eleanor I Sams, Rachel Slaugh, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2025
Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p SyndromesYingxi Wang, Eleanor I Sams, Rachel Slaugh, et al.
Science (New York, N.Y.)|May 26, 2009
Antigenic and genetic characteristics of swine-origin 2009 A(H1N1) influenza viruses circulating in humansRebecca J Garten, C Todd Davis, Colin A Russell, et al.
Science Translational Medicine|May 31, 2023
PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon productionFrédéric Ebstein, Sébastien Küry, Victoria Most, et al.
Human Mutation|March 19, 2013
Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domainPartha Sen, Yaping Yang, Colby Navarro, et al.
JAMA Pediatrics|February 28, 2017
Families as Partners in Hospital Error and Adverse Event SurveillanceAlisa Khan, Maitreya Coffey, Katherine P Litterer, et al.
Nature Methods|February 9, 2026
Addressing pandemic-wide systematic errors in the SARS-CoV-2 phylogenyMartin Hunt, Angie S Hinrichs, Daniel Anderson, et al.
Biorxiv : the Preprint Server for Biology|May 15, 2024
Addressing pandemic-wide systematic errors in the SARS-CoV-2 phylogenyMartin Hunt, Angie S Hinrichs, Daniel Anderson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Pageof 96