A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27
- 1 October 2002
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 71 (4) , 777-790
- https://doi.org/10.1086/342720
Abstract
No abstract availableKeywords
This publication has 61 references indexed in Scilit:
- Phenotypic Homogeneity Provides Increased Support for Linkage on Chromosome 2 in Autistic DisorderAmerican Journal of Human Genetics, 2002
- Genomic screen and follow‐up analysis for autistic disorderAmerican Journal of Medical Genetics, 2001
- Evidence for a Susceptibility Gene for Autism on Chromosome 2 and for Genetic HeterogeneityAmerican Journal of Human Genetics, 2001
- Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15American Journal of Human Genetics, 2000
- The SPCH1 Region on Human 7q31: Genomic Characterization of the Critical Interval and Localization of Translocations Associated with Speech and Language DisorderAmerican Journal of Human Genetics, 2000
- Gamete-Competition ModelsAmerican Journal of Human Genetics, 2000
- Genetic Studies of Autistic Disorder and Chromosome 7Genomics, 1999
- A Genomic Screen of Autism: Evidence for a Multilocus EtiologyAmerican Journal of Human Genetics, 1999
- A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism ConsortiumHuman Molecular Genetics, 1998
- Linkage probability and its approximate confidence interval under possible heterogeneityGenetic Epidemiology, 1986