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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: larizza l. 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: larizza l. Cancer Genet Cytogenet. 2000 Jun;119(2):102-8. doi: 10.1016/s0165-4608(99)00222-8. Cancer Genet Cytogenet. 2000. PMID: 10867143
297 results