Executive functioning in preschoolers with 22q11.2 deletion syndrome and the impact of congenital heart defects

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource, 1 online resource.

Language: Englisch

Bibliographic citation: Executive functioning in preschoolers with 22q11.2 deletion syndrome and the impact of congenital heart defects ; volume:15 ; number:1 ; day:13 ; month:5 ; year:2023 ; pages:1-19 ; date:12.2023
Journal of neurodevelopmental disorders ; 15, Heft 1 (13.5.2023), 1-19, 12.2023

Creator: Everaert, Emma
Vorstman, Jacob A. S.
Selten, Iris S.
Slieker, Martijn G.
Wijnen, Frank
Boerma, Tessel D.
Houben, Michiel L.

Contributor: SpringerLink (Online service)

DOI: 10.1186/s11689-023-09484-y

URN: urn:nbn:de:101:1-2023090812301476081656

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:45 AM CEST

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Everaert, Emma
Vorstman, Jacob A. S.
Selten, Iris S.
Slieker, Martijn G.
Wijnen, Frank
Boerma, Tessel D.
Houben, Michiel L.
SpringerLink (Online service)

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Executive functioning in preschoolers with 22q11.2 deletion syndrome and the impact of congenital heart defects

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Other Objects (12)

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

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Genotype-phenotype correlation in 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Episodic Future Thinking in Autism Spectrum Disorder and 22q11.2 Deletion Syndrome: Association with Anticipatory Pleasure and Social Functioning

Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes

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Complement Activation in 22q11.2 Deletion Syndrome

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Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome

Genotype-phenotype correlation in 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Episodic Future Thinking in Autism Spectrum Disorder and 22q11.2 Deletion Syndrome: Association with Anticipatory Pleasure and Social Functioning

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Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

Complement Activation in 22q11.2 Deletion Syndrome

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Genotype-phenotype correlation in 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

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