Portal de Periódicos da CAPES

De novo 13q31.1-q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2

2013; Wiley; Volume: 161; Issue: 4 Linguagem: Inglês

10.1002/ajmg.a.35781

1552-4833

Elisa Tassano, Maja Di Rocco, Sara Signa, Giorgio Gimelli,

RNA regulation and disease

American Journal of Medical Genetics Part AVolume 161, Issue 4 p. 894-896 Research Letter De novo 13q31.1–q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2†‡ E. Tassano Ph.D., Corresponding Author E. Tassano Ph.D. eli.tassano@gmail.com elisatassano@ospedale-gaslini.ge.it Laboratorio di Citogenetica, Istituto G. Gaslini, Genova, ItalyLaboratorio di Citogenetica, Istituto G.Gaslini, Largo G.Gaslini 5, I-16148 Genova, Italy.Search for more papers by this authorM. Di Rocco, M. Di Rocco Unit of Rare Diseases, Department of Pediatrics, Istituto G. Gaslini, Genova, ItalySearch for more papers by this authorS. Signa, S. Signa Unit of Rare Diseases, Department of Pediatrics, Istituto G. Gaslini, Genova, ItalySearch for more papers by this authorG. Gimelli, G. Gimelli Laboratorio di Citogenetica, Istituto G. Gaslini, Genova, ItalySearch for more papers by this author E. Tassano Ph.D., Corresponding Author E. Tassano Ph.D. eli.tassano@gmail.com elisatassano@ospedale-gaslini.ge.it Laboratorio di Citogenetica, Istituto G. Gaslini, Genova, ItalyLaboratorio di Citogenetica, Istituto G.Gaslini, Largo G.Gaslini 5, I-16148 Genova, Italy.Search for more papers by this authorM. Di Rocco, M. Di Rocco Unit of Rare Diseases, Department of Pediatrics, Istituto G. Gaslini, Genova, ItalySearch for more papers by this authorS. Signa, S. Signa Unit of Rare Diseases, Department of Pediatrics, Istituto G. Gaslini, Genova, ItalySearch for more papers by this authorG. Gimelli, G. Gimelli Laboratorio di Citogenetica, Istituto G. Gaslini, Genova, ItalySearch for more papers by this author First published: 12 March 2013 https://doi.org/10.1002/ajmg.a.35781Citations: 18 † All the authors have no conflict of interest to declare. ‡ How to Cite this Article: Tassano E, Di Rocco M, Signa S, Gimelli G. 2013. De novo 13q31.1–q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2. Am J Med Genet Part A 161A:894–896 Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume161, Issue4April 2013Pages 894-896 RelatedInformation