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Christopher M Watson

Showing results (51-60 of 94) with videos related to

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Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|February 19, 2026
Reconsidering Pediatric Critical Care Sequencing: A Qualitative Exploration of Postgraduate Year 1 PICU Rotations Among Senior Pediatric ResidentsRachel R Johnson, Kiersten Flodman, Brooke Lichak, et al.
Plos One|November 3, 2011
Characterizing hospital workers' willingness to respond to a radiological eventRan D Balicer, Christina L Catlett, Daniel J Barnett, et al.
Human Mutation|June 4, 2015
Rapid Detection of Rare Deleterious Variants by Next Generation Sequencing with Optional Microarray SNP Genotype DataChristopher M Watson, Laura A Crinnion, Juliana Gurgel-Gianetti, et al.
Molecular Genetics & Genomic Medicine|January 8, 2016
A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencingJames A Poulter, Claire E L Smith, Gina Murrillo, et al.
American Journal of Medical Genetics. Part A|July 22, 2014
Diagnostic whole genome sequencing and split-read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndromeChristopher M Watson, Laura A Crinnion, Antigoni Tzika, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 29, 2020
Assessing the utility of long-read nanopore sequencing for rapid and efficient characterization of mobile element insertionsChristopher M Watson, Laura A Crinnion, Helen Lindsay, et al.
Human Mutation|April 14, 2025
The Common <i>PKD1</i> p.(Ile3167Phe) Variant Is Hypomorphic and Associated with Very Early Onset, Biallelic Polycystic Kidney DiseaseMiranda Durkie, Christopher M Watson, Peter Winship, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|March 6, 2025
Acute Respiratory Distress Syndrome in Children With Lower Respiratory Tract Infection Requiring Invasive Mechanical Ventilation: Post Hoc Analysis of the 2019-2020 Bronchiolitis and Codetection CohortBenjamin R White, Lee Polikoff, Robin Alexander, et al.
Human Mutation|December 6, 2013
Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interfaceChristopher M Watson, Laura A Crinnion, Joanne E Morgan, et al.
Journal of Medical Genetics|October 30, 2021
Molecular diagnoses in the congenital malformations caused by ciliopathies cohort of the 100,000 Genomes ProjectSunayna Best, Jenny Lord, Matthew Roche, et al.
Pageof 10

Showing results (51-60 of 94) with videos related to

Sort By:
Pageof 10
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|February 19, 2026
Reconsidering Pediatric Critical Care Sequencing: A Qualitative Exploration of Postgraduate Year 1 PICU Rotations Among Senior Pediatric ResidentsRachel R Johnson, Kiersten Flodman, Brooke Lichak, et al.
Plos One|November 3, 2011
Characterizing hospital workers' willingness to respond to a radiological eventRan D Balicer, Christina L Catlett, Daniel J Barnett, et al.
Human Mutation|June 4, 2015
Rapid Detection of Rare Deleterious Variants by Next Generation Sequencing with Optional Microarray SNP Genotype DataChristopher M Watson, Laura A Crinnion, Juliana Gurgel-Gianetti, et al.
Molecular Genetics & Genomic Medicine|January 8, 2016
A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencingJames A Poulter, Claire E L Smith, Gina Murrillo, et al.
American Journal of Medical Genetics. Part A|July 22, 2014
Diagnostic whole genome sequencing and split-read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndromeChristopher M Watson, Laura A Crinnion, Antigoni Tzika, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 29, 2020
Assessing the utility of long-read nanopore sequencing for rapid and efficient characterization of mobile element insertionsChristopher M Watson, Laura A Crinnion, Helen Lindsay, et al.
Human Mutation|April 14, 2025
The Common <i>PKD1</i> p.(Ile3167Phe) Variant Is Hypomorphic and Associated with Very Early Onset, Biallelic Polycystic Kidney DiseaseMiranda Durkie, Christopher M Watson, Peter Winship, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|March 6, 2025
Acute Respiratory Distress Syndrome in Children With Lower Respiratory Tract Infection Requiring Invasive Mechanical Ventilation: Post Hoc Analysis of the 2019-2020 Bronchiolitis and Codetection CohortBenjamin R White, Lee Polikoff, Robin Alexander, et al.
Human Mutation|December 6, 2013
Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interfaceChristopher M Watson, Laura A Crinnion, Joanne E Morgan, et al.
Journal of Medical Genetics|October 30, 2021
Molecular diagnoses in the congenital malformations caused by ciliopathies cohort of the 100,000 Genomes ProjectSunayna Best, Jenny Lord, Matthew Roche, et al.
Pageof 10