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Maartje J Vogel

Showing results (1-10 of 13) with videos related to

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Nature Protocols|June 5, 2007
Detection of in vivo protein-DNA interactions using DamID in mammalian cellsMaartje J Vogel, Daniel Peric-Hupkes, Bas van Steensel
Epigenetics & Chromatin|January 31, 2009
High-resolution mapping of heterochromatin redistribution in a Drosophila position-effect variegation modelMaartje J Vogel, Ludo Pagie, Wendy Talhout, et al.
Ecancermedicalscience|December 1, 2016
Next-generation sequencing in NSCLC and melanoma patients: a cost and budget impact analysisRosa A van Amerongen, Valesca P Retèl, Veerle Mh Coupé, et al.
Genome Research|October 14, 2006
Human heterochromatin proteins form large domains containing KRAB-ZNF genesMaartje J Vogel, Lars Guelen, Elzo de Wit, et al.
American Journal of Medical Genetics. Part A|October 12, 2013
Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS-FREM complex disordersDenny Schanze, Magdalena Harakalova, Cathy A Stevens, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Discovery of variants unmasked by hemizygous deletionsRon Hochstenbach, Martin Poot, Isaac J Nijman, et al.
Journal of Medical Genetics|April 19, 2012
Mutations in GRIP1 cause Fraser syndromeMaartje J Vogel, Patrick van Zon, Louise Brueton, et al.
Human Mutation|June 19, 2013
Best practice guidelines for the use of next-generation sequencing applications in genome diagnostics: a national collaborative study of Dutch genome diagnostic laboratoriesMarjan M Weiss, Bert Van der Zwaag, Jan D H Jongbloed, et al.
Frontiers in Radiology|June 3, 2026
Case Report: Epidermal growth factor receptor germline variant associated with epilepsy and rare, distinctive cerebral MRI abnormalitiesElise A Ferreira, Machteld M Oud, Erik-Jan Kamsteeg, et al.
Human Mutation|August 22, 2019
Dutch genome diagnostic laboratories accelerated and improved variant interpretation and increased accuracy by sharing dataIvo F A C Fokkema, Kasper J van der Velde, Mariska K Slofstra, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Nature Protocols|June 5, 2007
Detection of in vivo protein-DNA interactions using DamID in mammalian cellsMaartje J Vogel, Daniel Peric-Hupkes, Bas van Steensel
Epigenetics & Chromatin|January 31, 2009
High-resolution mapping of heterochromatin redistribution in a Drosophila position-effect variegation modelMaartje J Vogel, Ludo Pagie, Wendy Talhout, et al.
Ecancermedicalscience|December 1, 2016
Next-generation sequencing in NSCLC and melanoma patients: a cost and budget impact analysisRosa A van Amerongen, Valesca P Retèl, Veerle Mh Coupé, et al.
Genome Research|October 14, 2006
Human heterochromatin proteins form large domains containing KRAB-ZNF genesMaartje J Vogel, Lars Guelen, Elzo de Wit, et al.
American Journal of Medical Genetics. Part A|October 12, 2013
Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS-FREM complex disordersDenny Schanze, Magdalena Harakalova, Cathy A Stevens, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Discovery of variants unmasked by hemizygous deletionsRon Hochstenbach, Martin Poot, Isaac J Nijman, et al.
Journal of Medical Genetics|April 19, 2012
Mutations in GRIP1 cause Fraser syndromeMaartje J Vogel, Patrick van Zon, Louise Brueton, et al.
Human Mutation|June 19, 2013
Best practice guidelines for the use of next-generation sequencing applications in genome diagnostics: a national collaborative study of Dutch genome diagnostic laboratoriesMarjan M Weiss, Bert Van der Zwaag, Jan D H Jongbloed, et al.
Frontiers in Radiology|June 3, 2026
Case Report: Epidermal growth factor receptor germline variant associated with epilepsy and rare, distinctive cerebral MRI abnormalitiesElise A Ferreira, Machteld M Oud, Erik-Jan Kamsteeg, et al.
Human Mutation|August 22, 2019
Dutch genome diagnostic laboratories accelerated and improved variant interpretation and increased accuracy by sharing dataIvo F A C Fokkema, Kasper J van der Velde, Mariska K Slofstra, et al.
Pageof 2