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Biological Psychiatry
|
March 25, 2022
The Hunt for the Chromosome 22q11.2 Deletion Syndrome Schizophrenia Genes
Joris Robert Vermeesch
European Journal of Human Genetics : EJHG
|
June 1, 2006
Reply to Hochstenbach et al. 'Molecular karyotyping'
Joris Robert Vermeesch, Anita Rauch
Genes
|
November 24, 2022
The 22q11.2 Low Copy Repeats
Lisanne Vervoort, Joris Robert Vermeesch
Clinical Chemistry
|
May 18, 2022
Commentary on Multiple Copy Number Variants Detected by Noninvasive Prenatal Testing
Joris Robert Vermeesch, Liesbeth Lenaerts
Prenatal Diagnosis
|
November 19, 2016
Current controversies in prenatal diagnosis 3: industry drives innovation in research and clinical application of genetic prenatal diagnosis and screening
Mark I Evans, Joris Robert Vermeesch
Nature Reviews. Genetics
|
September 16, 2016
Prenatal and pre-implantation genetic diagnosis
Joris 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 Amplification
Eftychia Dimitriadou, Masoud Zamani Esteki, Joris Robert Vermeesch
Prenatal Diagnosis
|
March 6, 2019
Current Controversies in Prenatal Diagnosis 3: Gene editing should replace embryo selection following PGD
Dagan Wells, Joris Robert Vermeesch, Joe Leigh Simpson
Nature Genetics
|
October 16, 2025
Expanding the scope of non-invasive prenatal screening
Kate Elizabeth Stanley, Bernard Thienpont, Joris Robert Vermeesch
Genome Medicine
|
July 31, 2010
Piecing together the problems in diagnosing low-level chromosomal mosaicism
Caroline Robberecht, Jean-Pierre Fryns, Joris Robert Vermeesch
Page
of 13
Search research articles
Search
Showing results (1-10 of 121) with videos related to
Sort By:
Page
of 13
Biological Psychiatry
|
March 25, 2022
The Hunt for the Chromosome 22q11.2 Deletion Syndrome Schizophrenia Genes
Joris Robert Vermeesch
European Journal of Human Genetics : EJHG
|
June 1, 2006
Reply to Hochstenbach et al. 'Molecular karyotyping'
Joris Robert Vermeesch, Anita Rauch
Genes
|
November 24, 2022
The 22q11.2 Low Copy Repeats
Lisanne Vervoort, Joris Robert Vermeesch
Clinical Chemistry
|
May 18, 2022
Commentary on Multiple Copy Number Variants Detected by Noninvasive Prenatal Testing
Joris Robert Vermeesch, Liesbeth Lenaerts
Prenatal Diagnosis
|
November 19, 2016
Current controversies in prenatal diagnosis 3: industry drives innovation in research and clinical application of genetic prenatal diagnosis and screening
Mark I Evans, Joris Robert Vermeesch
Nature Reviews. Genetics
|
September 16, 2016
Prenatal and pre-implantation genetic diagnosis
Joris 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 Amplification
Eftychia Dimitriadou, Masoud Zamani Esteki, Joris Robert Vermeesch
Prenatal Diagnosis
|
March 6, 2019
Current Controversies in Prenatal Diagnosis 3: Gene editing should replace embryo selection following PGD
Dagan Wells, Joris Robert Vermeesch, Joe Leigh Simpson
Nature Genetics
|
October 16, 2025
Expanding the scope of non-invasive prenatal screening
Kate Elizabeth Stanley, Bernard Thienpont, Joris Robert Vermeesch
Genome Medicine
|
July 31, 2010
Piecing together the problems in diagnosing low-level chromosomal mosaicism
Caroline Robberecht, Jean-Pierre Fryns, Joris Robert Vermeesch
Page
of 13