Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion

Por Gagliardi, C, Bonaglia, M, Selicorni, A, Borgatti, R, Giorda, R
Publicado em 2003

Trisomy 10qter confirmed by in situ hybridisation.

Por Briscioli, V, Floridia, G, Rossi, E, Selicorni, A, Lalatta, F, Zuffardi, O
Publicado em 1993

Peripheral blood cells from children with RASopathies show enhanced spontaneous colonies growth in vitro and hyperactive RAS signaling

Por Gaipa, G, Bugarin, C, Cianci, P, Sarno, J, Bonaccorso, P, Biondi, A, Selicorni, A
Publicado no Blood Cancer J (2015)

Cornelia de Lange Syndrome: NIPBL haploinsufficiency downregulates canonical Wnt pathway in zebrafish embryos and patients fibroblasts

Por Pistocchi, A, Fazio, G, Cereda, A, Ferrari, L, Bettini, L R, Messina, G, Cotelli, F, Biondi, A, Selicorni, A, Massa, V
Publicado em 2013

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

Por Silibello, G., Vizziello, P., Gallucci, M., Selicorni, A., Milani, D., Ajmone, P. F., Rigamonti, C., De Stefano, S., Bedeschi, M. F., Lalatta, Faustina
Publicado no Ital J Pediatr (2016)