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E Fry

Showing results (601-610 of 649) with videos related to

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BMJ Open|January 12, 2022
Problems with evidence assessment in COVID-19 health policy impact evaluation: a systematic review of study design and evidence strengthNoah A Haber, Emma Clarke-Deelder, Avi Feller, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2021
Problems with Evidence Assessment in COVID-19 Health Policy Impact Evaluation: A systematic review of study design and evidence strengthNoah A Haber, Emma Clarke-Deelder, Avi Feller, et al.
BMC Medical Genetics|April 27, 2016
Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsyAndrew E Fry, Elliott Rees, Rose Thompson, et al.
European Journal of Human Genetics : EJHG|June 26, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
Science (New York, N.Y.)|January 26, 1996
Molecular cloning and disease association of hepatitis G virus: a transfusion-transmissible agentJ Linnen, J Wages, Z Y Zhang-Keck, et al.
Plant Physiology|February 15, 2003
Comparative analyses of potato expressed sequence tag librariesCatherine M Ronning, Svetlana S Stegalkina, Robert A Ascenzi, et al.
Journal of Medical Genetics|April 8, 2022
Overlapping cortical malformations in patients with pathogenic variants in <i>GRIN1</i> and <i>GRIN2B</i>Stefanie Brock, Annie Laquerriere, Florent Marguet, et al.
American Journal of Human Genetics|October 23, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal FeaturesPeter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
Nature Methods|June 20, 2017
High-speed fixed-target serial virus crystallographyPhilip Roedig, Helen M Ginn, Tim Pakendorf, et al.
Pageof 65

Showing results (601-610 of 649) with videos related to

Sort By:
Pageof 65
BMJ Open|January 12, 2022
Problems with evidence assessment in COVID-19 health policy impact evaluation: a systematic review of study design and evidence strengthNoah A Haber, Emma Clarke-Deelder, Avi Feller, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2021
Problems with Evidence Assessment in COVID-19 Health Policy Impact Evaluation: A systematic review of study design and evidence strengthNoah A Haber, Emma Clarke-Deelder, Avi Feller, et al.
BMC Medical Genetics|April 27, 2016
Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsyAndrew E Fry, Elliott Rees, Rose Thompson, et al.
European Journal of Human Genetics : EJHG|June 26, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
Science (New York, N.Y.)|January 26, 1996
Molecular cloning and disease association of hepatitis G virus: a transfusion-transmissible agentJ Linnen, J Wages, Z Y Zhang-Keck, et al.
Plant Physiology|February 15, 2003
Comparative analyses of potato expressed sequence tag librariesCatherine M Ronning, Svetlana S Stegalkina, Robert A Ascenzi, et al.
Journal of Medical Genetics|April 8, 2022
Overlapping cortical malformations in patients with pathogenic variants in <i>GRIN1</i> and <i>GRIN2B</i>Stefanie Brock, Annie Laquerriere, Florent Marguet, et al.
American Journal of Human Genetics|October 23, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal FeaturesPeter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
Nature Methods|June 20, 2017
High-speed fixed-target serial virus crystallographyPhilip Roedig, Helen M Ginn, Tim Pakendorf, et al.
Pageof 65