Pages that link to "Q48612697"
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The following pages link to Enlarged sylvian fissures in infants with interstitial deletion of chromosome 22q11 (Q48612697):
Displaying 11 items.
- Mapping cortical thickness in children with 22q11.2 deletions (Q33644926) (← links)
- Regional cortical volumes and congenital heart disease: a MRI study in 22q11.2 deletion syndrome (Q34284040) (← links)
- Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome (Q35054138) (← links)
- Patterns of dysmorphic features in schizophrenia (Q35124133) (← links)
- Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia (Q35748140) (← links)
- Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome. (Q35809309) (← links)
- Insights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and velocardiofacial syndrome (Q37450139) (← links)
- Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome. (Q37480286) (← links)
- Synchronous Aberrant Cerebellar and Opercular Development in Fetuses and Neonates with Congenital Heart Disease: Correlation with Early Communicative Neurodevelopmental Outcomes, Initial Experience (Q37639109) (← links)
- Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome. (Q46408355) (← links)
- Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome (Q48504162) (← links)