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Cell|February 25, 2017
Mutational Processes Shaping the Genome in Early Human EmbryosThierry Voet, Joris R VermeeschGenome Medicine|September 4, 2013
Preimplantation genetic diagnosis guided by single-cell genomicsNiels Van der Aa, Masoud Zamani Esteki, Joris R Vermeesch, et al.Genome Biology|August 23, 2011
Single-cell copy number variation detectionJiqiu Cheng, Evelyne Vanneste, Peter Konings, et al.Genome Research|December 6, 2012
Nonallelic homologous recombination between retrotransposable elements is a driver of de novo unbalanced translocationsCaroline Robberecht, Thierry Voet, Masoud Zamani Esteki, et al.Molecular Cytogenetics|July 31, 2014
Single cell segmental aneuploidy detection is compromised by S phaseEftychia Dimitriadou, Niels Van der Aa, Jiqiu Cheng, et al.Current Genomics|March 2, 2011
Somatic genomic variations in early human prenatal developmentCaroline Robberecht, Evelyne Vanneste, Anne Pexsters, et al.Human Reproduction (Oxford, England)|July 28, 2009
What next for preimplantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rateEvelyne Vanneste, Thierry Voet, Cindy Melotte, et al.Nucleic Acids Research|February 25, 2022
Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencingHeleen Masset, Jia Ding, Eftychia Dimitriadou, et al.Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|March 2, 2017
How can zygotes segregate entire parental genomes into distinct blastomeres? The zygote metaphase revisitedAspasia Destouni, Joris R VermeeschHuman Genomics|December 17, 2004
Chromosomal phenotypes and submicroscopic abnormalitiesKoen Devriendt, Joris R VermeeschPageof 25