Presence of Large Deletions in Kindreds with Autism
- 1 July 2002
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 71 (1) , 100-115
- https://doi.org/10.1086/341291
Abstract
No abstract availableKeywords
This publication has 56 references indexed in Scilit:
- The DNA sequence and comparative analysis of human chromosome 20Nature, 2001
- Linkage Disequilibrium at the Angelman Syndrome Gene UBE3A in Autism FamiliesGenomics, 2001
- Assessment of the Total Number of Human Transcription UnitsGenomics, 2001
- Creation of genome-wide protein expression libraries using random activation of gene expressionNature Biotechnology, 2001
- Cloning and Characterization of a Golgin-Related Gene from the Large-Scale Polymorphism Linked to the PML GeneGenomics, 2000
- Genetic studies in autistic disorder and chromosome 15neurogenetics, 2000
- Association study with two markers of a human homeogene in infantile autism.Journal of Medical Genetics, 1995
- The PML gene is linked to a megabase-scale insertion/deletion restriction fragment length polymorphismGenomics, 1995
- Case reports of autism with interstitial deletion of chromosome 17 (p11.2 p11.2) and monosomy of chromosome 5 (5pter → 5p 15.3)Psychiatric Genetics, 1994
- Partial 6p trisomy associated with infantile autismClinical Genetics, 1988