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Joke Verheij

Showing results (1-10 of 9) with videos related to

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The British Journal of Educational Psychology|December 16, 2003
Learning styles: self-reports versus thinking-aloud measuresMarcel V J Veenman, Frans J Prins, Joke Verheij
Prenatal Diagnosis|November 8, 2019
Is there still a role for nuchal translucency measurement in the changing paradigm of first trimester screening?Francesca Bardi, Pien Bosschieter, Joke Verheij, et al.
NPJ Genomic Medicine|May 4, 2024
Reply to: Pitfalls in the genetic testing of the OPN1LW-OPN1MW gene cluster in human subjectsLonneke Haer-Wigman, Amber den Ouden, Ronny Derks, et al.
Prenatal Diagnosis|October 13, 2021
Parental experiences of rapid exome sequencing in cases with major ultrasound anomalies during pregnancyMirjam Plantinga, Lauren Zwienenberg, Eva van Dijk, et al.
European Journal of Human Genetics : EJHG|May 13, 2004
Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2Grzegorz M Burzynski, Ilja M Nolte, Jan Osinga, et al.
Ophthalmology|August 31, 2010
Simultaneous mutation detection in 90 retinal disease genes in multiple patients using a custom-designed 300-kb retinal resequencing chipJudith C Booij, Arne Bakker, Jamilia Kulumbetova, et al.
European Journal of Human Genetics : EJHG|July 24, 2008
Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotypeMaria Clara Bonaglia, Roberto Ciccone, Giorgio Gimelli, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysisIlse Feenstra, Nicolien Hanemaaijer, Birgit Sikkema-Raddatz, et al.
NPJ Genomic Medicine|November 9, 2022
Diagnostic analysis of the highly complex OPN1LW/OPN1MW gene cluster using long-read sequencing and MLPALonneke Haer-Wigman, Amber den Ouden, Maria M van Genderen, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
The British Journal of Educational Psychology|December 16, 2003
Learning styles: self-reports versus thinking-aloud measuresMarcel V J Veenman, Frans J Prins, Joke Verheij
Prenatal Diagnosis|November 8, 2019
Is there still a role for nuchal translucency measurement in the changing paradigm of first trimester screening?Francesca Bardi, Pien Bosschieter, Joke Verheij, et al.
NPJ Genomic Medicine|May 4, 2024
Reply to: Pitfalls in the genetic testing of the OPN1LW-OPN1MW gene cluster in human subjectsLonneke Haer-Wigman, Amber den Ouden, Ronny Derks, et al.
Prenatal Diagnosis|October 13, 2021
Parental experiences of rapid exome sequencing in cases with major ultrasound anomalies during pregnancyMirjam Plantinga, Lauren Zwienenberg, Eva van Dijk, et al.
European Journal of Human Genetics : EJHG|May 13, 2004
Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2Grzegorz M Burzynski, Ilja M Nolte, Jan Osinga, et al.
Ophthalmology|August 31, 2010
Simultaneous mutation detection in 90 retinal disease genes in multiple patients using a custom-designed 300-kb retinal resequencing chipJudith C Booij, Arne Bakker, Jamilia Kulumbetova, et al.
European Journal of Human Genetics : EJHG|July 24, 2008
Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotypeMaria Clara Bonaglia, Roberto Ciccone, Giorgio Gimelli, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysisIlse Feenstra, Nicolien Hanemaaijer, Birgit Sikkema-Raddatz, et al.
NPJ Genomic Medicine|November 9, 2022
Diagnostic analysis of the highly complex OPN1LW/OPN1MW gene cluster using long-read sequencing and MLPALonneke Haer-Wigman, Amber den Ouden, Maria M van Genderen, et al.
Pageof 1