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Pediatric Pulmonology
|
December 17, 2008
Strategic plan for pediatric respiratory diseases research: an NHLBI working group report
Steve Abman, Alan Jobe, Victor Chernick, et al.
The New England Journal of Medicine
|
November 6, 2014
Changes in medical errors after implementation of a handoff program
Amy J Starmer, Nancy D Spector, Rajendu Srivastava, et al.
JAMA Pediatrics
|
September 27, 2021
Effect of Whole-Genome Sequencing on the Clinical Management of Acutely Ill Infants With Suspected Genetic Disease: A Randomized Clinical Trial
, Ian D Krantz, Livija Medne, et al.
The New England Journal of Medicine
|
June 7, 2013
The OHRP and SUPPORT
Benjamin S Wilfond, David Magnus, Armand H Antommaria, et al.
Human Mutation
|
March 3, 2016
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients
Bobby 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 syndromes
Yingxi 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 Syndromes
Yingxi Wang, Eleanor I Sams, Rachel Slaugh, et al.
Science Translational Medicine
|
May 31, 2023
PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production
Frédéric 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 domain
Partha Sen, Yaping Yang, Colby Navarro, et al.
JAMA Pediatrics
|
February 28, 2017
Families as Partners in Hospital Error and Adverse Event Surveillance
Alisa Khan, Maitreya Coffey, Katherine P Litterer, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 101) with videos related to
Sort By:
Page
of 11
Pediatric Pulmonology
|
December 17, 2008
Strategic plan for pediatric respiratory diseases research: an NHLBI working group report
Steve Abman, Alan Jobe, Victor Chernick, et al.
The New England Journal of Medicine
|
November 6, 2014
Changes in medical errors after implementation of a handoff program
Amy J Starmer, Nancy D Spector, Rajendu Srivastava, et al.
JAMA Pediatrics
|
September 27, 2021
Effect of Whole-Genome Sequencing on the Clinical Management of Acutely Ill Infants With Suspected Genetic Disease: A Randomized Clinical Trial
, Ian D Krantz, Livija Medne, et al.
The New England Journal of Medicine
|
June 7, 2013
The OHRP and SUPPORT
Benjamin S Wilfond, David Magnus, Armand H Antommaria, et al.
Human Mutation
|
March 3, 2016
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients
Bobby 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 syndromes
Yingxi 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 Syndromes
Yingxi Wang, Eleanor I Sams, Rachel Slaugh, et al.
Science Translational Medicine
|
May 31, 2023
PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production
Frédéric 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 domain
Partha Sen, Yaping Yang, Colby Navarro, et al.
JAMA Pediatrics
|
February 28, 2017
Families as Partners in Hospital Error and Adverse Event Surveillance
Alisa Khan, Maitreya Coffey, Katherine P Litterer, et al.
Page
of 11