Pages that link to "Q48812843"

The following pages link to A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome (Q48812843):

Displaying 16 items.

• Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes (Q30472917) (← links)
• Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome (Q33710925) (← links)
• Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)? (Q35280963) (← links)
• An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome (Q35599290) (← links)
• Deficits in mental state attributions in individuals with 22q11.2 deletion syndrome (velo-cardio-facial syndrome). (Q36484359) (← links)
• Action simulation in hallucination-prone adolescents (Q36981645) (← links)
• Social cognition in 22q11.2 microdeletion syndrome: relevance to psychosis? (Q37021707) (← links)
• Visual memory profile in 22q11.2 microdeletion syndrome: are there differences in performance and neurobiological substrates between tasks linked to ventral and dorsal visual brain structures? A cross-sectional and longitudinal study (Q37408865) (← links)
• Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes. (Q37716526) (← links)
• Visual processing of emotional dynamic faces in 22q11.2 deletion syndrome (Q47597196) (← links)
• Social cognition dysfunction in adolescents with 22q11.2 deletion syndrome (velo-cardio-facial syndrome): relationship with executive functioning and social competence/functioning. (Q47738547) (← links)
• Negative subthreshold psychotic symptoms distinguish 22q11.2 deletion syndrome from other neurodevelopmental disorders: A two-site study (Q47839388) (← links)
• Intellectual functioning in relation to autism and ADHD symptomatology in children and adolescents with 22q11.2 deletion syndrome (Q48327735) (← links)
• The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome. (Q48462197) (← links)
• Neuropsychological profile of Italian children and adolescents with 22q11.2 deletion syndrome with and without intellectual disability (Q50789313) (← links)
• Laterality Preference and Cognition: Cross-Syndrome Comparison of Patients with Trisomy 21 (Down), del7q11.23 (Williams–Beuren) and del22q11.2 (DiGeorge or Velo-Cardio-Facial) Syndromes (Q58198898) (← links)