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A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MT, Melis D, Manfredini E, Ferrero GB, Pecile V, Larizza L. Russo S, et al. Among authors: miozzo m. Clin Epigenetics. 2016 Mar 1;8:23. doi: 10.1186/s13148-016-0183-8. eCollection 2016. Clin Epigenetics. 2016. PMID: 26933465 Free PMC article.
19p deletion in recurring leiomyosarcoma lesions from the same patient.
Riva P, Dalprá L, Gualandri V, Volontè M, Miozzo M, Malgara R, Conti AF, Larizza L. Riva P, et al. Among authors: miozzo m. Cancer Genet Cytogenet. 2000 Jun;119(2):102-8. doi: 10.1016/s0165-4608(99)00222-8. Cancer Genet Cytogenet. 2000. PMID: 10867143
X monosomy in female systemic lupus erythematosus.
Invernizzi P, Miozzo M, Oertelt-Prigione S, Meroni PL, Persani L, Selmi C, Battezzati PM, Zuin M, Lucchi S, Marasini B, Zeni S, Watnik M, Tabano S, Maitz S, Pasini S, Gershwin ME, Podda M. Invernizzi P, et al. Among authors: miozzo m. Ann N Y Acad Sci. 2007 Sep;1110:84-91. doi: 10.1196/annals.1423.010. Ann N Y Acad Sci. 2007. PMID: 17911423
Misbehaviour of XIST RNA in breast cancer cells.
Sirchia SM, Tabano S, Monti L, Recalcati MP, Gariboldi M, Grati FR, Porta G, Finelli P, Radice P, Miozzo M. Sirchia SM, et al. Among authors: miozzo m. PLoS One. 2009;4(5):e5559. doi: 10.1371/journal.pone.0005559. Epub 2009 May 15. PLoS One. 2009. PMID: 19440381 Free PMC article.
233 results