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Joris R Vermeesch

Showing results (1-10 of 168) with videos related to

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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 Vermeesch
Cell|February 25, 2017
Mutational Processes Shaping the Genome in Early Human EmbryosThierry Voet, Joris R Vermeesch
Human Genomics|December 17, 2004
Chromosomal phenotypes and submicroscopic abnormalitiesKoen Devriendt, Joris R Vermeesch
American Journal of Medical Genetics. Part A|July 2, 2003
Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1-->q27)Joris R Vermeesch, Jean-Pierre Fryns
Prenatal Diagnosis|April 3, 2012
Genomic microarrays: a technology overviewPaul D Brady, Joris R Vermeesch
Prenatal Diagnosis|July 21, 2018
Response to a comment on "Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing"Nathalie Brison, Luc Dehaspe, Joris R Vermeesch
Prenatal Diagnosis|February 1, 2021
Genome-wide abnormalities in embryos: Origins and clinical consequencesHeleen Masset, Olga Tšuiko, Joris R Vermeesch
European Journal of Medical Genetics|September 24, 2005
25 Mb deletion of 13q13.3-->q21.31 in a patient without retinoblastomaBernard Thienpont, Joris R Vermeesch, Jean-Pierre Fryns
European Journal of Medical Genetics|March 4, 2010
Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delayFemke Hannes, Malgorzata Drozniewska, Joris R Vermeesch, et al.
Genome Biology|December 16, 2021
A benchmark of structural variation detection by long reads through a realistic simulated modelNicolas Dierckxsens, Tong Li, Joris R Vermeesch, et al.
Pageof 17

Showing results (1-10 of 168) with videos related to

Sort By:
Pageof 17
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 Vermeesch
Cell|February 25, 2017
Mutational Processes Shaping the Genome in Early Human EmbryosThierry Voet, Joris R Vermeesch
Human Genomics|December 17, 2004
Chromosomal phenotypes and submicroscopic abnormalitiesKoen Devriendt, Joris R Vermeesch
American Journal of Medical Genetics. Part A|July 2, 2003
Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1-->q27)Joris R Vermeesch, Jean-Pierre Fryns
Prenatal Diagnosis|April 3, 2012
Genomic microarrays: a technology overviewPaul D Brady, Joris R Vermeesch
Prenatal Diagnosis|July 21, 2018
Response to a comment on "Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing"Nathalie Brison, Luc Dehaspe, Joris R Vermeesch
Prenatal Diagnosis|February 1, 2021
Genome-wide abnormalities in embryos: Origins and clinical consequencesHeleen Masset, Olga Tšuiko, Joris R Vermeesch
European Journal of Medical Genetics|September 24, 2005
25 Mb deletion of 13q13.3-->q21.31 in a patient without retinoblastomaBernard Thienpont, Joris R Vermeesch, Jean-Pierre Fryns
European Journal of Medical Genetics|March 4, 2010
Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delayFemke Hannes, Malgorzata Drozniewska, Joris R Vermeesch, et al.
Genome Biology|December 16, 2021
A benchmark of structural variation detection by long reads through a realistic simulated modelNicolas Dierckxsens, Tong Li, Joris R Vermeesch, et al.
Pageof 17