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Page 1
Wolfram's syndrome and HLA.
Mattina T, Li Volti S, Palmeri P, Tribulato A, Salerno A, Mollica F. Mattina T, et al. Ophthalmic Paediatr Genet. 1988 Mar;9(1):25-8. doi: 10.3109/13816818809031477. Ophthalmic Paediatr Genet. 1988. PMID: 3043304 Review.
Mutational spectrum and clinical signatures in 114 families with hereditary multiple osteochondromas: insights into molecular properties of selected exostosin variants.
Fusco C, Nardella G, Fischetto R, Copetti M, Petracca A, Annunziata F, Augello B, D'Asdia MC, Petrucci S, Mattina T, Rella A, Cassina M, Bengala M, Biagini T, Causio FA, Caldarini C, Brancati F, De Luca A, Guarnieri V, Micale L, D'Agruma L, Castori M. Fusco C, et al. Among authors: mattina t. Hum Mol Genet. 2019 Jul 1;28(13):2133-2142. doi: 10.1093/hmg/ddz046. Hum Mol Genet. 2019. PMID: 30806661
Unstable translocations: a new case?
Mattina T, Milana G, D'Agata A, Conti L, Sciacca F. Mattina T, et al. Clin Genet. 1991 Feb;39(2):149-50. doi: 10.1111/j.1399-0004.1991.tb03002.x. Clin Genet. 1991. PMID: 1826645
Mild cystic fibrosis in patients with the rare P5L CFTR mutation.
Spicuzza L, Sciuto C, Di Dio L, Mattina T, Leonardi S, del Giudice MM, La Rosa M. Spicuzza L, et al. Among authors: mattina t. J Cyst Fibros. 2012 Jan;11(1):30-3. doi: 10.1016/j.jcf.2011.08.009. Epub 2011 Oct 7. J Cyst Fibros. 2012. PMID: 21983161 Free article.
Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform.
Calì F, Chiavetta V, Ruggeri G, Piccione M, Selicorni A, Palazzo D, Bonsignore M, Cereda A, Elia M, Failla P, Figura MG, Fiumara A, Maitz S, Luana Mandarà GM, Mattina T, Ragalmuto A, Romano C, Ruggieri M, Salluzzo R, Saporoso A, Schepis C, Sorge G, Spanò M, Tortorella G, Romano V. Calì F, et al. Among authors: mattina t. Eur J Med Genet. 2017 Feb;60(2):93-99. doi: 10.1016/j.ejmg.2016.11.001. Epub 2016 Nov 9. Eur J Med Genet. 2017. PMID: 27838393
83 results