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Microdeletion 2q23.3q24.1: exploring genotype-phenotype correlations.
Milani D, Sabatini C, Manzoni FM, Ajmone PF, Rigamonti C, Malacarne M, Pierluigi M, Cavani S, Costantino MA. Milani D, et al. Among authors: ajmone pf. Congenit Anom (Kyoto). 2015 May;55(2):107-11. doi: 10.1111/cga.12080. Congenit Anom (Kyoto). 2015. PMID: 25174267
Daily life changes and adaptations investigated in 154 families with a child suffering from a rare disability at a public centre for rare diseases in Northern Italy.
Silibello G, Vizziello P, Gallucci M, Selicorni A, Milani D, Ajmone PF, Rigamonti C, De Stefano S, Bedeschi MF, Lalatta F. Silibello G, et al. Among authors: ajmone pf. Ital J Pediatr. 2016 Aug 31;42(1):76. doi: 10.1186/s13052-016-0285-0. Ital J Pediatr. 2016. PMID: 27576488 Free PMC article.
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith-Wiedemann syndrome.
Fontana L, Bedeschi MF, Cagnoli GA, Costanza J, Persico N, Gangi S, Porro M, Ajmone PF, Colapietro P, Santaniello C, Crippa M, Sirchia SM, Miozzo M, Tabano S. Fontana L, et al. Among authors: ajmone pf. Mol Genet Genomic Med. 2020 Sep;8(9):e1386. doi: 10.1002/mgg3.1386. Epub 2020 Jul 6. Mol Genet Genomic Med. 2020. PMID: 32627967 Free PMC article.
Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations.
Villa R, Fergnani VGC, Silipigni R, Guerneri S, Cinnante C, Guala A, Danesino C, Scola E, Conte G, Fumagalli M, Gangi S, Colombo L, Picciolini O, Ajmone PF, Accogli A, Madia F, Tassano E, Scala M, Capra V, Srour M, Spaccini L, Righini A, Greco D, Castiglia L, Romano C, Bedeschi MF. Villa R, et al. Among authors: ajmone pf. Eur J Paediatr Neurol. 2020 Sep;28:110-119. doi: 10.1016/j.ejpn.2020.07.002. Epub 2020 Jul 28. Eur J Paediatr Neurol. 2020. PMID: 32800423 Free article.
36 results