Familial Dyslexia: Use of Genetic Linkage Data to Define Subtypes
- 1 March 1990
- journal article
- research article
- Published by Elsevier in Journal of the American Academy of Child & Adolescent Psychiatry
- Vol. 29 (2), 204-213
- https://doi.org/10.1097/00004583-199003000-00008
Abstract
No abstract availableKeywords
This publication has 47 references indexed in Scilit:
- Converging evidence for multiple genetic forms of reading disabilityBrain and Language, 1988
- Evidence for a genetic aetiology in reading disability of twinsNature, 1987
- Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6Clinical Genetics, 1987
- Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish materialClinical Genetics, 1987
- Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17Science, 1987
- Genetic linkage between X-chromosome markers and bipolar affective illnessNature, 1987
- Close linkage of c-Harvey-ras-1 and the insulin gene to affective disorder is ruled out in three North American pedigreesNature, 1987
- Developmental Dyslexia: a Diagnostic Approach Based on Three Atypical Reading‐spelling PatternsDevelopmental Medicine and Child Neurology, 1973
- RESEARCH IN READING RETARDATION: TWO CRITICAL PROBLEMS *Journal of Child Psychology and Psychiatry, 1971
- DyslexiaJournal of Learning Disabilities, 1969