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Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum.
Front Genet. 2023 Jul 17;14:1198821. doi: 10.3389/fgene.2023.1198821. eCollection 2023.
Front Genet. 2023.
PMID: 37529781
Free PMC article.
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith-Wiedemann progeny.
Tannorella P, Calzari L, Daolio C, Mainini E, Vimercati A, Gentilini D, Soli F, Pedrolli A, Bonati MT, Larizza L, Russo S.
Tannorella P, et al. Among authors: vimercati a.
Clin Epigenetics. 2022 Mar 22;14(1):43. doi: 10.1186/s13148-022-01262-2.
Clin Epigenetics. 2022.
PMID: 35317853
Free PMC article.
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Modeling RTT Syndrome by iPSC-Derived Neurons from Male and Female Patients with Heterogeneously Severe Hot-Spot MECP2 Variants.
Perego S, Alari V, Pietra G, Lamperti A, Vimercati A, Camporeale N, Garzo M, Cogliati F, Milani D, Vignoli A, Peron A, Larizza L, Pizzorusso T, Russo S.
Perego S, et al. Among authors: vimercati a.
Int J Mol Sci. 2022 Nov 21;23(22):14491. doi: 10.3390/ijms232214491.
Int J Mol Sci. 2022.
PMID: 36430969
Free PMC article.
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Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases.
Tannorella P, Minervino D, Guzzetti S, Vimercati A, Calzari L, Patti G, Maghnie M, Allegri AEM, Milani D, Scuvera G, Mariani M, Modena P, Selicorni A, Larizza L, Russo S.
Tannorella P, et al. Among authors: vimercati a.
Genes (Basel). 2021 Apr 17;12(4):588. doi: 10.3390/genes12040588.
Genes (Basel). 2021.
PMID: 33920573
Free PMC article.
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