Pages that link to "Q52179872"
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The following pages link to Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern. (Q52179872):
Displaying 50 items.
- Genetic Syndromes associated with Congenital Heart Disease (Q26786025) (← links)
- Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome (Q26824150) (← links)
- Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion Syndrome (Q28081645) (← links)
- Communication disorders in the 22Q11.2 microdeletion syndrome (Q28141568) (← links)
- Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications (Q28200131) (← links)
- Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes (Q28254095) (← links)
- Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders (Q30439224) (← links)
- The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders (Q30468033) (← links)
- Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes (Q30472917) (← links)
- 22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia (Q30478713) (← links)
- Factors affecting articulation skills in children with velocardiofacial syndrome and children with cleft palate or velopharyngeal dysfunction: a preliminary report (Q30479967) (← links)
- Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice (Q30481665) (← links)
- Evidence for involvement of GNB1L in autism (Q30504581) (← links)
- 22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases (Q30619280) (← links)
- Feasibility and preliminary efficacy data from a computerized cognitive intervention in children with chromosome 22q11.2 deletion syndrome (Q30644398) (← links)
- Cognitive characteristics of children with genetic syndromes (Q31115382) (← links)
- A new account of the neurocognitive foundations of impairments in space, time and number processing in children with chromosome 22q11.2 deletion syndrome (Q31162000) (← links)
- Associations between performance on the Rey-Osterrieth Complex Figure and regional brain volumes in children with and without velocardiofacial syndrome (Q33561889) (← links)
- Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence (Q33581309) (← links)
- MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q (Q33622853) (← links)
- The importance of understanding cognitive trajectories: the case of 22q11.2 deletion syndrome (Q33629249) (← links)
- Mapping cortical thickness in children with 22q11.2 deletions (Q33644926) (← links)
- Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory (Q33675258) (← links)
- Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome (Q33710925) (← links)
- Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland (Q33763901) (← links)
- Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome (Q33863797) (← links)
- CHARGE (coloboma, heart defect, atresia choanae, retarded growth and development, genital hypoplasia, ear anomalies/deafness) syndrome and chromosome 22q11.2 deletion syndrome: a comparison of immunologic and nonimmunologic phenotypic features (Q33903396) (← links)
- Mouse Models of 22q11.2-Associated Autism Spectrum Disorder (Q33988040) (← links)
- Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome (Q33999011) (← links)
- Discrepancies in parent and teacher ratings of social-behavioral functioning of children with chromosome 22q11.2 deletion syndrome: implications for assessment (Q34013379) (← links)
- Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: a 3-year follow-up study (Q34054916) (← links)
- 22q11.2 deletion syndrome: are motor deficits more than expected for IQ level? (Q34116641) (← links)
- Socioeconomic Status and Psychological Function in Children with Chromosome 22q11.2 Deletion Syndrome: Implications for Genetic Counseling (Q34154742) (← links)
- Long-term developmental outcome of children with complex congenital heart disease (Q34193766) (← links)
- Prenatal diagnosis of the 22q11.2 deletion syndrome (Q34242714) (← links)
- Taking advantage of early diagnosis: preschool children with the 22q11.2 deletion (Q34242734) (← links)
- A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children (Q34334067) (← links)
- Is child intelligence associated with parent and sibling intelligence in individuals with developmental disorders? An investigation in youth with 22q11.2 deletion (velo-cardio-facial) syndrome (Q34620870) (← links)
- Recent developments in the application of the nonverbal learning disabilities model (Q34856227) (← links)
- Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome (Q35054138) (← links)
- Neurocognitive profile in 22q11 deletion syndrome and schizophrenia (Q35081406) (← links)
- Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype? (Q35083203) (← links)
- Developmental malformation of the corpus callosum: a review of typical callosal development and examples of developmental disorders with callosal involvement (Q35187186) (← links)
- Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome (Q35499123) (← links)
- An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome (Q35599290) (← links)
- Syndromic immunodeficiencies: genetic syndromes associated with immune abnormalities (Q35621987) (← links)
- Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and at-risk for psychosis (Q35738055) (← links)
- A cross-sectional study of the development of volitional control of spatial attention in children with chromosome 22q11.2 deletion syndrome (Q36028885) (← links)
- Annotation: velo-cardio-facial syndrome (Q36118609) (← links)
- A biologic model to study the genetics of psychotic, mood, and anxiety disorders: the velocardiofacial syndrome (Q36422281) (← links)