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
Adolescents | 1 |
Children | 1 |
Congenital Impairments | 1 |
Genetic Disorders | 1 |
Genetics | 1 |
Matched Groups | 1 |
Memory | 1 |
Risk | 1 |
Schizophrenia | 1 |
Source
Research in Developmental… | 1 |
Author
Frangou, Sophia | 1 |
Habel, Alex | 1 |
Jacobson, Clare | 1 |
Kravariti, Eugenia | 1 |
Morris, Robin | 1 |
Murray, Robin M. | 1 |
Shearer, Jo | 1 |
Tsakanikos, Elias | 1 |
Publication Type
Journal Articles | 1 |
Reports - Research | 1 |
Education Level
Audience
Location
Laws, Policies, & Programs
Assessments and Surveys
What Works Clearinghouse Rating
Kravariti, Eugenia; Jacobson, Clare; Morris, Robin; Frangou, Sophia; Murray, Robin M.; Tsakanikos, Elias; Habel, Alex; Shearer, Jo – Research in Developmental Disabilities: A Multidisciplinary Journal, 2010
The 22q11.2 deletion syndrome (22qDS) and schizophrenia have genetic and neuropsychological similarities, but are likely to differ in memory profile. Confirming differences in memory function between the two disorders, and identifying their genetic determinants, can help to define genetic subtypes in both syndromes, identify genetic risk factors…
Descriptors: Memory, Schizophrenia, Congenital Impairments, Genetic Disorders