Boccuto, Luigi
Boccuto, Luigi
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Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders.
2013 Boccuto, Luigi; Lauri, Maria; Sarasua, Sm; Skinner, Cd; Buccella, D; Dwivedi, A; Zollino, Marcella; Orteschi, Daniela; Visconti, P; Dupont, B; Tiziano, Francesco Danilo; Schroer, Rj; Neri, Giovanni; Stevenson, Re; Gurrieri, Fiorella; Schwartz, Ce; Collins, Js
Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder
2009 Gurrieri, Fiorella; Neri, Giovanni; Boccuto, Luigi
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.
2008 Sparago, A; Verde, G; De Crescenzo, A; Citro, V; Cubellis, Mv; Rinaldi, Mm; Boccuto, Luigi; Neri, Giovanni; Magnani, C; D'Angelo, P; Collini, P; Perotti, D; Sebastio, G; Maher, R; Riccio, A.
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2013 | Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders. | Boccuto, Luigi; Lauri, Maria; Sarasua, Sm; Skinner, Cd; Buccella, D; Dwivedi, A; Zollino, Marcella; Orteschi, Daniela; Visconti, P; Dupont, B; Tiziano, Francesco Danilo; Schroer, Rj; Neri, Giovanni; Stevenson, Re; Gurrieri, Fiorella; Schwartz, Ce; Collins, Js | |
| 1-gen-2009 | Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder | Gurrieri, Fiorella; Neri, Giovanni; Boccuto, Luigi | |
| 1-gen-2008 | Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour. | Sparago, A; Verde, G; De Crescenzo, A; Citro, V; Cubellis, Mv; Rinaldi, Mm; Boccuto, Luigi; Neri, Giovanni; Magnani, C; D'Angelo, P; Collini, P; Perotti, D; Sebastio, G; Maher, R; Riccio, A. |