Publication Date
In 2025 | 0 |
Since 2024 | 0 |
Since 2021 (last 5 years) | 0 |
Since 2016 (last 10 years) | 0 |
Since 2006 (last 20 years) | 1 |
Descriptor
Source
Research in Developmental… | 1 |
Author
Brown, Scott | 1 |
Campbell, Linda E. | 1 |
Hammond, Peter | 1 |
Murphy, Declan G. M. | 1 |
Murphy, Kieran C. | 1 |
Schall, Ulrich | 1 |
Sinderberry, Brooke | 1 |
Stevens, Angela F. | 1 |
Publication Type
Journal Articles | 1 |
Reports - Research | 1 |
Education Level
Audience
Location
Laws, Policies, & Programs
Assessments and Surveys
What Works Clearinghouse Rating
Sinderberry, Brooke; Brown, Scott; Hammond, Peter; Stevens, Angela F.; Schall, Ulrich; Murphy, Declan G. M.; Murphy, Kieran C.; Campbell, Linda E. – Research in Developmental Disabilities: A Multidisciplinary Journal, 2013
22q11.2 deletion syndrome (22q11DS) has a complex phenotype with more than 180 characteristics, including cardiac anomalies, cleft palate, intellectual disabilities, a typical facial morphology, and mental health problems. However, the variable phenotype makes it difficult to predict clinical outcome, such as the high prevalence of psychosis among…
Descriptors: Disability Identification, Mental Health, Congenital Impairments, Executive Function