F. Cavalleri

Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutation

G. Scarano, A. Bentivegna, A. Selicorni, 2007, Clinical genetics.

Prenatal/neonatal pathology in two cases of Cornelia de Lange syndrome harboring novel mutations of NIPBL

A. Bentivegna, F. Lalatta, L. Larizza, 2007, Genetics in Medicine.

Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes

W. Roberts, M. Elia, L. Larizza, 2007, Neurogenetics.

A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith-Wiedemann syndrome.

A. Selicorni, L. Larizza, S. Russo, 2003, Molecular and cellular probes.

Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian family.

D. Toniolo, G. Casari, L. Larizza, 2000, American journal of medical genetics.

Novel mutations of ubiquitin protein ligase 3A gene in Italian patients with Angelman syndrome

A. Selicorni, M. Viri, A. Romeo, 2000, Human mutation.