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Chiari 1 malformation and exome sequencing in 51 trios: the emerging role of rare missense variants in chromatin-remodeling genes.
Provenzano A, La Barbera A, Scagnet M, Pagliazzi A, Traficante G, Pantaleo M, Tiberi L, Vergani D, Kurtas NE, Guarducci S, Bargiacchi S, Forzano G, Artuso R, Palazzo V, Kura A, Giordano F, di Feo D, Mortilla M, De Filippi C, Mattei G, Garavelli L, Giusti B, Genitori L, Zuffardi O, Giglio S. Provenzano A, et al. Among authors: genitori l. Hum Genet. 2021 Apr;140(4):625-647. doi: 10.1007/s00439-020-02231-6. Epub 2020 Dec 18. Hum Genet. 2021. PMID: 33337535 Free PMC article.
Craniofacial surgery in fibrous dysplasia.
Giordano F, Serio P, Savasta S, Oliveri G, Genitori L. Giordano F, et al. Among authors: genitori l. J Pediatr Endocrinol Metab. 2006 May;19 Suppl 2:595-604. doi: 10.1515/jpem.2006.19.s2.595. J Pediatr Endocrinol Metab. 2006. PMID: 16789622
Intracerebral atypical presentation of echinococcosis in a child.
Sardi I, Sanzo M, Buccoliero AM, Mortilla M, de Martino M, Genitori L. Sardi I, et al. Among authors: genitori l. Pediatr Neurosurg. 2008;44(4):350-2. doi: 10.1159/000138376. Epub 2008 Jun 13. Pediatr Neurosurg. 2008. PMID: 18552521 Review. No abstract available.
165 results