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Wouter Steyaert

Showing results (1-10 of 37) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|August 29, 2018
BATCH-GE: Analysis of NGS Data for Genome Editing AssessmentWouter Steyaert, Annekatrien Boel, Paul Coucke, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|May 29, 2021
Comprehensive validation of a diagnostic strategy for sequencing genes with one or multiple pseudogenes using pseudoxanthoma elasticum as a modelWouter Steyaert, Shana Verschuere, Paul J Coucke, et al.
Acta Clinica Belgica|February 1, 2018
Future perspectives of genome-scale sequencingWouter Steyaert, Steven Callens, Paul Coucke, et al.
Disease Markers|October 28, 2015
Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian FamilyDelfien Syx, Sofie Symoens, Wouter Steyaert, et al.
Journal of Genetic Counseling|April 13, 2024
Accepting or declining preconception expanded carrier screening: An exploratory study with 407 couplesAriane J A G Van Tongerloo, Hannah Verdin, Wouter Steyaert, et al.
Disease Models & Mechanisms|October 26, 2018
CRISPR/Cas9-mediated homology-directed repair by ssODNs in zebrafish induces complex mutational patterns resulting from genomic integration of repair-template fragmentsAnnekatrien Boel, Hanna De Saffel, Wouter Steyaert, et al.
Scientific Reports|October 31, 2018
Publisher Correction: BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessmentAnnekatrien Boel, Wouter Steyaert, Nina De Rocker, et al.
American Journal of Medical Genetics. Part A|March 7, 2017
Tissue-specific mosaicism for a lethal osteogenesis imperfecta COL1A1 mutation causes mild OI/EDS overlap syndromeSofie Symoens, Wouter Steyaert, Lynn Demuynck, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 27, 2022
Hypergastrinemia, a clue leading to the identification of an atypical form of diabetes mellitus type 2Wouter Steyaert, Matthew J Varney, Jeffrey L Benovic, et al.
Neurology|April 5, 2015
RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorderPatrick Santens, Tim Van Damme, Wouter Steyaert, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Methods in Molecular Biology (Clifton, N.J.)|August 29, 2018
BATCH-GE: Analysis of NGS Data for Genome Editing AssessmentWouter Steyaert, Annekatrien Boel, Paul Coucke, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|May 29, 2021
Comprehensive validation of a diagnostic strategy for sequencing genes with one or multiple pseudogenes using pseudoxanthoma elasticum as a modelWouter Steyaert, Shana Verschuere, Paul J Coucke, et al.
Acta Clinica Belgica|February 1, 2018
Future perspectives of genome-scale sequencingWouter Steyaert, Steven Callens, Paul Coucke, et al.
Disease Markers|October 28, 2015
Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian FamilyDelfien Syx, Sofie Symoens, Wouter Steyaert, et al.
Journal of Genetic Counseling|April 13, 2024
Accepting or declining preconception expanded carrier screening: An exploratory study with 407 couplesAriane J A G Van Tongerloo, Hannah Verdin, Wouter Steyaert, et al.
Disease Models & Mechanisms|October 26, 2018
CRISPR/Cas9-mediated homology-directed repair by ssODNs in zebrafish induces complex mutational patterns resulting from genomic integration of repair-template fragmentsAnnekatrien Boel, Hanna De Saffel, Wouter Steyaert, et al.
Scientific Reports|October 31, 2018
Publisher Correction: BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessmentAnnekatrien Boel, Wouter Steyaert, Nina De Rocker, et al.
American Journal of Medical Genetics. Part A|March 7, 2017
Tissue-specific mosaicism for a lethal osteogenesis imperfecta COL1A1 mutation causes mild OI/EDS overlap syndromeSofie Symoens, Wouter Steyaert, Lynn Demuynck, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 27, 2022
Hypergastrinemia, a clue leading to the identification of an atypical form of diabetes mellitus type 2Wouter Steyaert, Matthew J Varney, Jeffrey L Benovic, et al.
Neurology|April 5, 2015
RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorderPatrick Santens, Tim Van Damme, Wouter Steyaert, et al.
Pageof 4