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Current Opinion in Psychiatry
|
January 19, 2016
The importance of understanding cognitive trajectories: the case of 22q11.2 deletion syndrome
Ann Swillen
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
May 20, 2015
Developmental trajectories in 22q11.2 deletion
Ann Swillen, Donna McDonald-McGinn
American Journal of Medical Genetics. Part A
|
April 27, 2018
Neurodevelopmental outcome in 22q11.2 deletion syndrome and management
Ann Swillen, Edward Moss, Sasja Duijff
Molecular Syndromology
|
February 6, 2020
Deep Phenotyping of Development, Communication and Behaviour in Phelan-McDermid Syndrome
Gilles Droogmans, Ann Swillen, Griet Van Buggenhout
Journal of Neurodevelopmental Disorders
|
June 19, 2025
Developmental milestones and cognitive trajectories in school-aged children with 16p11.2 deletion
Jente Verbesselt, Jeroen Breckpot, Inge Zink, et al.
Journal of Speech, Language, and Hearing Research : JSLHR
|
October 17, 2024
Language Profiles of School-Age Children With 16p11.2 Copy Number Variants in a Clinically Ascertained Cohort
Jente Verbesselt, Jeroen Breckpot, Inge Zink, et al.
American Journal of Medical Genetics. Part A
|
September 7, 2021
Cross-sectional and longitudinal findings in patients with proximal 22q11.2 duplication: A retrospective chart study
Jente Verbesselt, Inge Zink, Jeroen Breckpot, et al.
American Journal of Medical Genetics. Part A
|
February 13, 2017
High prevalence of fatigue in adults with a 22q11.2 deletion syndrome
Elfi Vergaelen, Stephan Claes, Stefan Kempke, et al.
Developmental Medicine and Child Neurology
|
December 8, 2022
Neurodevelopmental profile and stages of regression in Phelan-McDermid syndrome
Yumi Dille, Lieven Lagae, Ann Swillen, et al.
Journal of Applied Research in Intellectual Disabilities : JARID
|
February 1, 2021
Stressed parents, happy parents. An assessment of parenting stress and family quality of life in families with a child with Phelan-McDermid syndrome
Gilles Droogmans, Elfi Vergaelen, Griet Van Buggenhout, et al.
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of 10
Search research articles
Search
Showing results (1-10 of 98) with videos related to
Sort By:
Page
of 10
Current Opinion in Psychiatry
|
January 19, 2016
The importance of understanding cognitive trajectories: the case of 22q11.2 deletion syndrome
Ann Swillen
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
May 20, 2015
Developmental trajectories in 22q11.2 deletion
Ann Swillen, Donna McDonald-McGinn
American Journal of Medical Genetics. Part A
|
April 27, 2018
Neurodevelopmental outcome in 22q11.2 deletion syndrome and management
Ann Swillen, Edward Moss, Sasja Duijff
Molecular Syndromology
|
February 6, 2020
Deep Phenotyping of Development, Communication and Behaviour in Phelan-McDermid Syndrome
Gilles Droogmans, Ann Swillen, Griet Van Buggenhout
Journal of Neurodevelopmental Disorders
|
June 19, 2025
Developmental milestones and cognitive trajectories in school-aged children with 16p11.2 deletion
Jente Verbesselt, Jeroen Breckpot, Inge Zink, et al.
Journal of Speech, Language, and Hearing Research : JSLHR
|
October 17, 2024
Language Profiles of School-Age Children With 16p11.2 Copy Number Variants in a Clinically Ascertained Cohort
Jente Verbesselt, Jeroen Breckpot, Inge Zink, et al.
American Journal of Medical Genetics. Part A
|
September 7, 2021
Cross-sectional and longitudinal findings in patients with proximal 22q11.2 duplication: A retrospective chart study
Jente Verbesselt, Inge Zink, Jeroen Breckpot, et al.
American Journal of Medical Genetics. Part A
|
February 13, 2017
High prevalence of fatigue in adults with a 22q11.2 deletion syndrome
Elfi Vergaelen, Stephan Claes, Stefan Kempke, et al.
Developmental Medicine and Child Neurology
|
December 8, 2022
Neurodevelopmental profile and stages of regression in Phelan-McDermid syndrome
Yumi Dille, Lieven Lagae, Ann Swillen, et al.
Journal of Applied Research in Intellectual Disabilities : JARID
|
February 1, 2021
Stressed parents, happy parents. An assessment of parenting stress and family quality of life in families with a child with Phelan-McDermid syndrome
Gilles Droogmans, Elfi Vergaelen, Griet Van Buggenhout, et al.
Page
of 10