Suggestive linkage of developmental dyslexia to chromosome 1p34-p36
โ Scribed by M. Rabin; X.L. Wen; M. Hepburn; H.A. Lubs; E. Feldman; R. Duara
- Book ID
- 119066049
- Publisher
- The Lancet
- Year
- 1993
- Tongue
- English
- Weight
- 169 KB
- Volume
- 342
- Category
- Article
- ISSN
- 0140-6736
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Abstract Dyslexia is a common and genetically complex trait that manifests primarily as a reading disability independent of general intelligence and educational opportunity. Strong evidence for a dyslexia susceptibility locus on chromosome 1p34โp36 (near marker D1S199) was recently reported, and
The genome scan of the European-American schizophrenia families from the Human Genetics Initiative of the National Institute of Mental Health (NIMH) reported a suggestive linkage to chromosome 10p. Subsequently, Paterson and Petronis [1999] reported evidence for transmission ratio distortion on 10p