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Ann Swillen

Showing results (61-70 of 98) with videos related to

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Genes|January 21, 2023
Prenatal Screening and Diagnostic Considerations for 22q11.2 MicrodeletionsNatalie Blagowidow, Beata Nowakowska, Erica Schindewolf, et al.
Human Molecular Genetics|December 30, 2019
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic originsLisanne Vervoort, Wolfram Demaerel, Laura Y Rengifo, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversionDavid Porubsky, DongAhn Yoo, Philip C Dishuck, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2015
Practical guidelines for managing adults with 22q11.2 deletion syndromeWai Lun Alan Fung, Nancy J Butcher, Gregory Costain, et al.
Nature Communications|April 18, 2026
Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversionDavid Porubsky, DongAhn Yoo, Nidhi Koundinya, et al.
European Journal of Human Genetics : EJHG|August 20, 2025
MINDDS-connect: a federated data platform integrating biobanks for meta cohort building and analysisBenjamin Huremagic, Nishkala Sattanathan, Mathilde Geysens, et al.
Clinical Genetics|December 8, 2025
Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22-23 DeletionsTanner J Nelson, Daniel E McGinn, T Blaine Crowley, et al.
The British Journal of Psychiatry : the Journal of Mental Science|January 4, 2019
Low prevalence of substance use in people with 22q11.2 deletion syndromeClaudia Vingerhoets, Mathilde J F van Oudenaren, Oswald J N Bloemen, et al.
Research Square|January 9, 2026
Multicenter retrospective study on effectiveness, reported side effects, and cognitive outcomes of SSRIs in 22q11.2 deletion syndromeCaren Latrèche, Valentina Mancini, Marija Dvojakovska, et al.
Molecular Psychiatry|March 3, 2023
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophreniaJhih-Rong Lin, Yingjie Zhao, M Reza Jabalameli, et al.
Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:
Pageof 10
Genes|January 21, 2023
Prenatal Screening and Diagnostic Considerations for 22q11.2 MicrodeletionsNatalie Blagowidow, Beata Nowakowska, Erica Schindewolf, et al.
Human Molecular Genetics|December 30, 2019
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic originsLisanne Vervoort, Wolfram Demaerel, Laura Y Rengifo, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversionDavid Porubsky, DongAhn Yoo, Philip C Dishuck, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2015
Practical guidelines for managing adults with 22q11.2 deletion syndromeWai Lun Alan Fung, Nancy J Butcher, Gregory Costain, et al.
Nature Communications|April 18, 2026
Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversionDavid Porubsky, DongAhn Yoo, Nidhi Koundinya, et al.
European Journal of Human Genetics : EJHG|August 20, 2025
MINDDS-connect: a federated data platform integrating biobanks for meta cohort building and analysisBenjamin Huremagic, Nishkala Sattanathan, Mathilde Geysens, et al.
Clinical Genetics|December 8, 2025
Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22-23 DeletionsTanner J Nelson, Daniel E McGinn, T Blaine Crowley, et al.
The British Journal of Psychiatry : the Journal of Mental Science|January 4, 2019
Low prevalence of substance use in people with 22q11.2 deletion syndromeClaudia Vingerhoets, Mathilde J F van Oudenaren, Oswald J N Bloemen, et al.
Research Square|January 9, 2026
Multicenter retrospective study on effectiveness, reported side effects, and cognitive outcomes of SSRIs in 22q11.2 deletion syndromeCaren Latrèche, Valentina Mancini, Marija Dvojakovska, et al.
Molecular Psychiatry|March 3, 2023
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophreniaJhih-Rong Lin, Yingjie Zhao, M Reza Jabalameli, et al.
Pageof 10