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Genes|November 24, 2022
The 22q11.2 Low Copy RepeatsLisanne Vervoort, Joris Robert Vermeesch
Nature Reviews. Genetics|September 16, 2016
Prenatal and pre-implantation genetic diagnosisJoris Robert Vermeesch, Thierry Voet, Koenraad Devriendt
Methods in Molecular Biology (Clifton, N.J.)|September 17, 2015
Copy Number Variation Analysis by Array Analysis of Single Cells Following Whole Genome AmplificationEftychia Dimitriadou, Masoud Zamani Esteki, Joris Robert Vermeesch
Nature Genetics|October 16, 2025
Expanding the scope of non-invasive prenatal screeningKate Elizabeth Stanley, Bernard Thienpont, Joris Robert Vermeesch
Genome Medicine|July 31, 2010
Piecing together the problems in diagnosing low-level chromosomal mosaicismCaroline Robberecht, Jean-Pierre Fryns, Joris Robert Vermeesch
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2009
Diagnosis of miscarriages by molecular karyotyping: benefits and pitfallsCaroline Robberecht, Vicky Schuddinck, Jean-Pierre Fryns, et al.
Reproduction (Cambridge, England)|October 16, 2020
PREIMPLANTATION GENETIC TESTING: Single-cell technologies at the forefront of PGT and embryo researchOlga Tšuiko, Elia Fernandez Gallardo, Thierry Voet, et al.
Journal of Bioethical Inquiry|January 11, 2023
Expanded Non-invasive Prenatal Testing (NIPT) : Can the Child's Right to an Open Future Help Set the Scope?Zoë Claesen, Neeltje Crombag, Lidewij Henneman, et al.
Seminars in Reproductive Medicine|June 23, 2012
Aneuploidy and copy number variation in early human developmentEvelyne Vanneste, Niels Van der Aa, Thierry Voet, et al.
Journal of Assisted Reproduction and Genetics|June 15, 2024
Polygenic embryo screening: quo vadis?Maria Siermann, Joris Robert Vermeesch, Taneli Raivio, et al.
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