How to cite this article: Entesarian M, Carlsson B, Mansouri MR, Stattin E-L, Holmberg E, Golovleva I, Stefansson H, Klar J, Dahl N. 2009. A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish population. Am J Med Genet Part A 149A:380–386.
A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish population†
Article first published online: 11 FEB 2009
Copyright © 2009 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 149A, Issue 3, pages 380–386, March 2009
How to Cite
Entesarian, M., Carlsson, B., Mansouri, M. R., Stattin, E.-L., Holmberg, E., Golovleva, I., Stefansson, H., Klar, J. and Dahl, N. (2009), A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish population. Am. J. Med. Genet., 149A: 380–386. doi: 10.1002/ajmg.a.32663
- Issue published online: 24 FEB 2009
- Article first published online: 11 FEB 2009
- Manuscript Accepted: 20 OCT 2008
- Manuscript Received: 13 AUG 2008
- Swedish Research Council
- The Sävstaholm Society
- Torsten and Ragnar Söderbergs Fund
- Stiftelsen Drottning Silvias Jubileumsfond
- Uppsala University and Uppsala University Hospital
Additional supporting information may be found in the online version of this article.
|ajma_32663_sm_supplfig1.pdf||30K||Supporting Information Fig. 1: Schematic overview of the 36 kb interval on chromosome 10q22.1 restricted by FISH mapping. Relative positions of restriction sites and the probe used for Southern blot analysis are indicated. The dashed line indicate the telomeric breakpoint region restricted by Southern blot analysis.|
|ajma_32663_sm_supplfig2.pdf||688K||Supporting Information Fig. 2: Southern blot analysis of DNA from subject 2 and controls using the probe indicated in suppl. fig1. An aberrant fragment is detected in the carrier using restriction endonucleases Sph I, Nco I and Nde I.|
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