Genetic Mechanisms in Childhood Psychiatric Disorders
Open Access
- 1 September 1994
- journal article
- review article
- Published by Elsevier in Journal of the American Academy of Child & Adolescent Psychiatry
- Vol. 33 (7) , 921-938
- https://doi.org/10.1097/00004583-199409000-00001
Abstract
No abstract availableKeywords
Funding Information
- NIH and ADAMHA (MH00856, MH44843, MH49351, MH00508, NS16648, HD03008, RR00125, and RR06022)
This publication has 111 references indexed in Scilit:
- A point mutation in the FMR-1 gene associated with fragile X mental retardationNature Genetics, 1993
- Evidence for a genetic etiology in hyperactivity in childrenBehavior Genetics, 1992
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Absence of expression of the FMR-1 gene in fragile X syndromeCell, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- A TWIN STUDY OF GENETIC INFLUENCES ON READING AND SPELLING ABILITY AND DISABILITYJournal of Child Psychology and Psychiatry, 1987
- The Inheritance of Gilles de la Tourette's Syndrome and Associated BehaviorsNew England Journal of Medicine, 1986
- Biometrical genetic models of self-reported delinquent behavior: A twin studyBehavior Genetics, 1983
- Deletions of Chromosome 15 as a Cause of the Prader–Willi SyndromeNew England Journal of Medicine, 1981
- The investigation of linkage between a quantitative trait and a marker locusBehavior Genetics, 1972