Case report
Isochromosome 13 in a patient with childhood-onset schizophrenia, ADHD, and motor tic disorder
-
* Corresponding author: Sharon L Graw Sharon.Graw@ucdenver.edu
1 Department of Psychiatry, University of Colorado School of Medicine, Aurora, CO, USA
2 Colorado Genetics Laboratory, Department of Pathology, University of Colorado School of Medicine, Aurora, CO, USA
3 Department of Psychiatry and Behavioral Science, Children's Hospital Colorado, Aurora, CO, USA
4 Research Division, Veterans Affairs Medical Research Service, Denver, CO, USA
Molecular Cytogenetics 2012, 5:2 doi:10.1186/1755-8166-5-2
Published: 3 January 2012Additional files
Additional file 1:
Chromosome 13 CNV analysis of patient and father. CNV analysis indicates the presence of two copies of almost all chromosome 13 markers in the patient and her father.
Format: PDF Size: 114KB Download file
This file can be viewed with: Adobe Acrobat Reader
Additional file 2:
Affymetrix Whole-Genome Human SNP6.0 CNV analysis of MYT1L and NRXN1 genes. Analysis indicates that the patient and her parents have two copies of the MYT1L and NRXN1 genes.
Format: PDF Size: 52KB Download file
This file can be viewed with: Adobe Acrobat Reader
Additional file 3:
Affymetrix Whole-genome Human SNP6.0 analysis of chromosome 16. Analysis indicates that the patient and her parents have regions on chromosome 16 with reduced heterozygosity, and that no significant deletions or duplications are found.
Format: PDF Size: 17KB Download file
This file can be viewed with: Adobe Acrobat Reader
Additional file 4:
SNP analysis. SNPS were detected in DAOA and HTR2A genes of patient.
Format: PDF Size: 17KB Download file
This file can be viewed with: Adobe Acrobat Reader