Conflict of interest: none.
Clinical manifestations of Xq28 functional disomy involving MECP2 in one female and two male patients
Version of Record online: 23 MAY 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 7, pages 1779–1785, July 2013
How to Cite
2013. Clinical manifestations of Xq28 functional disomy involving MECP2 in one female and two male patients. Am J Med Genet Part A 161A:1779–1785., , , , , , , , .
- Issue online: 19 JUN 2013
- Version of Record online: 23 MAY 2013
- Manuscript Accepted: 12 MAR 2013
- Manuscript Received: 2 SEP 2012
- Ministry of Education, Culture, Sports, Science and Technology (MEXT)
- Ministry of Health, Labor, and Welfare, Japan
- Japan Society for the Promotion of Science
Additional supporting information may be found in the online version of this article at the publisher's web-site.
|ajmga35975-sm-0001-SupFig-S1.tif||2838K||Figure S1. Additional results of chromosomal microarray testing. (Top) Patient 1. Loss of genomic copy number in the subtelomeric region of 12q24.33 with a size of 1.4 Mb is shown. (Bottom) Patient 2. Loss of genomic copy number in the distal region of Yq11.22 is noted. Blue-translucent rectangles indicate aberrant regions. The results of these analyses are visualized using the Agilent Genomic Workbench ver 6.5 (Agilent Technologies).|
|ajmga35975-sm-0002-SupTab-S1.xls||33K||Table SI. List of the Genes Included in the Deletion Region of 12q24.33 in Patient 1.|
Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.