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Characterization of BRCA Deficiency in Ovarian Cancer.
Cancers (Basel). 2023 Feb 28;15(5):1530. doi: 10.3390/cancers15051530.
Cancers (Basel). 2023.
PMID: 36900320
Free PMC article.
Occurrence of complete arhinia in two siblings with a clinical picture of Treacher Collins syndrome negative for TCOF1, POLR1D and POLR1C mutations.
Cesaretti C, Gentilin B, Bianchi V, Melloni G, Bonaguro M, Rossi C, Meazzini C, Brusati R, Lalatta F.
Cesaretti C, et al. Among authors: bonaguro m.
Clin Dysmorphol. 2011 Oct;20(4):229-231. doi: 10.1097/MCD.0b013e3283491725.
Clin Dysmorphol. 2011.
PMID: 21772136
No abstract available.
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The Relevance of Family History Taking in the Detection and Management of Birt-Hogg-Dubé Syndrome.
Torricelli E, Occhipinti M, Cavigli E, Tancredi G, Rosi E, Rossi C, Bonaguro M, Candita L, Papi L, Novelli L, Bezzi M, Bargagli E, Voltolini L, Pistolesi M.
Torricelli E, et al. Among authors: bonaguro m.
Respiration. 2019;98(2):125-132. doi: 10.1159/000498973. Epub 2019 Jul 2.
Respiration. 2019.
PMID: 31266032
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SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations.
Lepri F, De Luca A, Stella L, Rossi C, Baldassarre G, Pantaleoni F, Cordeddu V, Williams BJ, Dentici ML, Caputo V, Venanzi S, Bonaguro M, Kavamura I, Faienza MF, Pilotta A, Stanzial F, Faravelli F, Gabrielli O, Marino B, Neri G, Silengo MC, Ferrero GB, Torrrente I, Selicorni A, Mazzanti L, Digilio MC, Zampino G, Dallapiccola B, Gelb BD, Tartaglia M.
Lepri F, et al. Among authors: bonaguro m.
Hum Mutat. 2011 Jul;32(7):760-72. doi: 10.1002/humu.21492. Epub 2011 Apr 28.
Hum Mutat. 2011.
PMID: 21387466
Free PMC article.
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