Atlas-based white matter analysis in individuals with velo-cardio-facial syndrome (22q11.2 deletion syndrome) and unaffected siblings

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1744-9081

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Atlas-based white matter analysis in individuals with velo-cardio-facial syndrome (22q11.2 deletion syndrome) and unaffected siblings ; volume:8 ; number:1 ; day:1 ; month:8 ; year:2012 ; pages:1-11 ; date:12.2012
Behavioral and brain functions ; 8, Heft 1 (1.8.2012), 1-11, 12.2012

Creator: Radoeva, Petya D.
Coman, Ioana L.
Antshel, Kevin M.
Fremont, Wanda
McCarthy, Christopher S.
Kotkar, Ashwini
Wang, Dongliang
Shprintzen, Robert J.
Kates, Wendy R.

Contributor: SpringerLink (Online service)

DOI: 10.1186/1744-9081-8-38

URN: urn:nbn:de:101:1-2021061720124227928119

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

Last update: 14.08.2025, 10:54 AM CEST

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Associated

Radoeva, Petya D.
Coman, Ioana L.
Antshel, Kevin M.
Fremont, Wanda
McCarthy, Christopher S.
Kotkar, Ashwini
Wang, Dongliang
Shprintzen, Robert J.
Kates, Wendy R.
SpringerLink (Online service)

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Atlas-based white matter analysis in individuals with velo-cardio-facial syndrome (22q11.2 deletion syndrome) and unaffected siblings

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Other Objects (12)

Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?

Complement Activation 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

Genotype-phenotype correlation in 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

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

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

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

Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome

Obesity and metabolic syndrome in adults with a 22q11.2 microdeletion

Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome

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Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?

Complement Activation 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

Genotype-phenotype correlation in 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

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

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

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

Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome

Obesity and metabolic syndrome in adults with a 22q11.2 microdeletion

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Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?

Complement Activation 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

Genotype-phenotype correlation in 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

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

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Obesity and metabolic syndrome in adults with a 22q11.2 microdeletion

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