Common inversion polymorphisms and rare microdeletions at 15q13.3
Open Access
- 15 October 2008
- journal article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 17 (2) , 149-150
- https://doi.org/10.1038/ejhg.2008.189
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Large recurrent microdeletions associated with schizophreniaNature, 2008
- Rare chromosomal deletions and duplications increase risk of schizophreniaNature, 2008
- The copy number variant involving part of the α7 nicotinic receptor gene contains a polymorphic inversionEuropean Journal of Human Genetics, 2008
- A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizuresNature Genetics, 2008
- Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromesGenome Biology, 2007
- High-Resolution Molecular Characterization of 15q11-q13 Rearrangements by Array Comparative Genomic Hybridization (Array CGH) with Detection of Gene DosageAmerican Journal of Human Genetics, 2004
- Genome architecture, rearrangements and genomic disordersTrends in Genetics, 2002