Contract grant sponsors: Fundació La Marató de TV3 (101130); FIS-program (I3SNS-CA10/01056); I3SNS Program of the Spanish Ministry of Health (CP03/0064; SIVI 1395/09); Fundacion Eugenio Rodriguez Pascual and the Instituto de Salud Carlos III (PI10/0148).
Genome-Wide Allelic Methylation Analysis Reveals Disease-Specific Susceptibility to Multiple Methylation Defects in Imprinting Syndromes
Article first published online: 19 FEB 2013
© 2013 Wiley Periodicals, Inc.
Volume 34, Issue 4, pages 595–602, April 2013
How to Cite
Court, F., Martin-Trujillo, A., Romanelli, V., Garin, I., Iglesias-Platas, I., Salafsky, I., Guitart, M., Perez de Nanclares, G., Lapunzina, P. and Monk, D. (2013), Genome-Wide Allelic Methylation Analysis Reveals Disease-Specific Susceptibility to Multiple Methylation Defects in Imprinting Syndromes. Hum. Mutat., 34: 595–602. doi: 10.1002/humu.22276
Communicated by Nancy B. Spinner
- Issue published online: 20 MAR 2013
- Article first published online: 19 FEB 2013
- Accepted manuscript online: 18 JAN 2013 09:50AM EST
- Manuscript Accepted: 7 JAN 2013
- Manuscript Received: 2 OCT 2012
- Fundació La Marató de TV3. Grant Number: 101130
- FIS-program. Grant Number: I3SNS-CA10/01056
- I3SNS Program of the Spanish Ministry of Health. Grant Numbers: CP03/0064, SIVI 1395/09
- Fundacion Eugenio Rodriguez Pascual and the Instituto de Salud Carlos III. Grant Number: PI10/0148
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