Abstract
Fragile X syndrome causes a spectrum of problems in the emotional, cognitive, and physical domains. Our knowledge of the FMR1 gene has improved our understanding of the phenotypic spectrum in this disorder. Molecular and clinical correlations and treatment issues are reviewed here.
Original language | English (US) |
---|---|
Pages (from-to) | 895-911 |
Number of pages | 17 |
Journal | Child and Adolescent Psychiatric Clinics of North America |
Volume | 5 |
Issue number | 4 |
State | Published - 1996 |
Externally published | Yes |
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Psychiatry and Mental health