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Screening of subtelomeric rearrangements in autistic disorder: identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocation.
Di Bella MA, Calì F, Seidita G, Mirisola M, Ragusa A, Ragalmuto A, Galesi O, Elia M, Greco D, Zingale M, Gambino G, D'Anna RP, Regan R, Carbone MC, Gallo A, Romano V. Di Bella MA, et al. Among authors: cali f. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):584-90. doi: 10.1002/ajmg.b.30328. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16823807
Analysis of the gastrin-releasing peptide receptor gene in Italian patients with autism spectrum disorders.
Seidita G, Mirisola M, D'Anna RP, Gallo A, Jensen RT, Mantey SA, Gonzalez N, Falco M, Zingale M, Elia M, Cucina L, Chiavetta V, Romano V, Cali F. Seidita G, et al. Among authors: cali f. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):807-13. doi: 10.1002/ajmg.b.30752. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18393381 Free article.
The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape.
Busby GB, Hellenthal G, Montinaro F, Tofanelli S, Bulayeva K, Rudan I, Zemunik T, Hayward C, Toncheva D, Karachanak-Yankova S, Nesheva D, Anagnostou P, Cali F, Brisighelli F, Romano V, Lefranc G, Buresi C, Ben Chibani J, Haj-Khelil A, Denden S, Ploski R, Krajewski P, Hervig T, Moen T, Herrera RJ, Wilson JF, Myers S, Capelli C. Busby GB, et al. Among authors: cali f. Curr Biol. 2015 Oct 5;25(19):2518-26. doi: 10.1016/j.cub.2015.08.007. Epub 2015 Sep 17. Curr Biol. 2015. PMID: 26387712 Free PMC 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. 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
105 results