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Ann Swillen

Showing results (51-60 of 98) with videos related to

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Orphanet Journal of Rare Diseases|August 18, 2025
Evaluating the relationship between caregiver depression, social support, and children's internalizing and externalizing symptoms in families affected by 22q11.2 deletion syndromeHolly Carbyn, Abiaz Hossain, Raquel L Dias, et al.
American Journal of Human Genetics|October 3, 2017
Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic RearrangementsWolfram Demaerel, Matthew S Hestand, Elfi Vergaelen, et al.
European Journal of Psychotraumatology|May 23, 2024
The mental health and traumatic experiences of mothers of children with 22q11DSAlexandra Finless, Andrea L Rideout, Ting Xiong, et al.
Nature Reviews. Disease Primers|May 19, 2016
22q11.2 deletion syndromeDonna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, et al.
Genome Research|November 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Biorxiv : the Preprint Server for Biology|April 2, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion SyndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Genes|January 21, 2023
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease ResearchLauren K White, T Blaine Crowley, Brenda Finucane, et al.
Human Genome Variation|June 9, 2016
A catalog of hemizygous variation in 127 22q11 deletion patientsMatthew S Hestand, Beata A Nowakowska, Elfi Vergaelen, et al.
Genome Research|September 5, 2019
The 22q11 low copy repeats are characterized by unprecedented size and structural variabilityWolfram Demaerel, Yulia Mostovoy, Feyza Yilmaz, et al.
Movement Disorders Clinical Practice|February 7, 2025
Prevalence of Parkinson's Disease in 22q11.2 Deletion Syndrome: A Multicenter StudyEmma N M M von Scheibler, Ann Swillen, Gabriela M Repetto, et al.
Pageof 10

Showing results (51-60 of 98) with videos related to

Sort By:
Pageof 10
Orphanet Journal of Rare Diseases|August 18, 2025
Evaluating the relationship between caregiver depression, social support, and children's internalizing and externalizing symptoms in families affected by 22q11.2 deletion syndromeHolly Carbyn, Abiaz Hossain, Raquel L Dias, et al.
American Journal of Human Genetics|October 3, 2017
Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic RearrangementsWolfram Demaerel, Matthew S Hestand, Elfi Vergaelen, et al.
European Journal of Psychotraumatology|May 23, 2024
The mental health and traumatic experiences of mothers of children with 22q11DSAlexandra Finless, Andrea L Rideout, Ting Xiong, et al.
Nature Reviews. Disease Primers|May 19, 2016
22q11.2 deletion syndromeDonna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, et al.
Genome Research|November 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Biorxiv : the Preprint Server for Biology|April 2, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion SyndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Genes|January 21, 2023
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease ResearchLauren K White, T Blaine Crowley, Brenda Finucane, et al.
Human Genome Variation|June 9, 2016
A catalog of hemizygous variation in 127 22q11 deletion patientsMatthew S Hestand, Beata A Nowakowska, Elfi Vergaelen, et al.
Genome Research|September 5, 2019
The 22q11 low copy repeats are characterized by unprecedented size and structural variabilityWolfram Demaerel, Yulia Mostovoy, Feyza Yilmaz, et al.
Movement Disorders Clinical Practice|February 7, 2025
Prevalence of Parkinson's Disease in 22q11.2 Deletion Syndrome: A Multicenter StudyEmma N M M von Scheibler, Ann Swillen, Gabriela M Repetto, et al.
Pageof 10