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Identification of three novel mutations in the CHD7 gene in patients with clinical signs of typical or atypical CHARGE syndrome.
Michelucci A, Ghirri P, Iacopetti P, Conidi ME, Fogli A, Baldinotti F, Lunardi S, Forli F, Moscuzza F, Berrettini S, Boldrini A, Simi P, Pellegrini S. Michelucci A, et al. Among authors: iacopetti p. Int J Pediatr Otorhinolaryngol. 2010 Dec;74(12):1441-4. doi: 10.1016/j.ijporl.2010.09.006. Epub 2010 Oct 12. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20943277
Gene symbol: CHD7. Disease: CHARGE syndrome.
Simi P, Michelucci A, Iacopetti P, Pellegrini S, Conidi ME. Simi P, et al. Among authors: iacopetti p. Hum Genet. 2008 Jun;123(5):549. Hum Genet. 2008. PMID: 20960640 No abstract available.
An RbAp48-like gene regulates adult stem cells in planarians.
Bonuccelli L, Rossi L, Lena A, Scarcelli V, Rainaldi G, Evangelista M, Iacopetti P, Gremigni V, Salvetti A. Bonuccelli L, et al. Among authors: iacopetti p. J Cell Sci. 2010 Mar 1;123(Pt 5):690-8. doi: 10.1242/jcs.053900. Epub 2010 Feb 2. J Cell Sci. 2010. PMID: 20124416 Free article.
21 results