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BMJ Open
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January 12, 2022
Problems with evidence assessment in COVID-19 health policy impact evaluation: a systematic review of study design and evidence strength
Noah 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 disorders
Ankur 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 strength
Noah 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 epilepsy
Andrew 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 disorders
Ankur 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 agent
J Linnen, J Wages, Z Y Zhang-Keck, et al.
Plant Physiology
|
February 15, 2003
Comparative analyses of potato expressed sequence tag libraries
Catherine 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 Features
Peter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
Nature Methods
|
June 20, 2017
High-speed fixed-target serial virus crystallography
Philip Roedig, Helen M Ginn, Tim Pakendorf, et al.
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of 65
Search research articles
Search
Showing results (601-610 of 649) with videos related to
Sort By:
Page
of 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 strength
Noah 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 disorders
Ankur 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 strength
Noah 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 epilepsy
Andrew 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 disorders
Ankur 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 agent
J Linnen, J Wages, Z Y Zhang-Keck, et al.
Plant Physiology
|
February 15, 2003
Comparative analyses of potato expressed sequence tag libraries
Catherine 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 Features
Peter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
Nature Methods
|
June 20, 2017
High-speed fixed-target serial virus crystallography
Philip Roedig, Helen M Ginn, Tim Pakendorf, et al.
Page
of 65