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Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
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March 2, 2017
How can zygotes segregate entire parental genomes into distinct blastomeres? The zygote metaphase revisited
Aspasia Destouni, Joris R Vermeesch
Cell
|
February 25, 2017
Mutational Processes Shaping the Genome in Early Human Embryos
Thierry Voet, Joris R Vermeesch
Human Genomics
|
December 17, 2004
Chromosomal phenotypes and submicroscopic abnormalities
Koen 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 overview
Paul 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 consequences
Heleen 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 retinoblastoma
Bernard 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 delay
Femke 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 model
Nicolas Dierckxsens, Tong Li, Joris R Vermeesch, et al.
Page
of 17
Search research articles
Search
Showing results (1-10 of 168) with videos related to
Sort By:
Page
of 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 revisited
Aspasia Destouni, Joris R Vermeesch
Cell
|
February 25, 2017
Mutational Processes Shaping the Genome in Early Human Embryos
Thierry Voet, Joris R Vermeesch
Human Genomics
|
December 17, 2004
Chromosomal phenotypes and submicroscopic abnormalities
Koen 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 overview
Paul 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 consequences
Heleen 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 retinoblastoma
Bernard 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 delay
Femke 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 model
Nicolas Dierckxsens, Tong Li, Joris R Vermeesch, et al.
Page
of 17