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Risultati: 1 - 4 di 4
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Documenti rinvenuti:
| Data di edizione | Titolo | Autore/i |
|---|---|---|
| 2019 | P37. Analysis of cortical gene expression variability in a mouse model of x-linked infantile spams syndrome | Verrillo, Lucia; Tuccillo, Mariacarmine; Drongitis, Denise; Mangano, Eleonora; Franco, Cristina; Terrone, Gaetano; Canzoniero, Lorella Maria Teresa; Del Giudice, Ennio; Bordoni, Roberta; Poeta, Loredana; Miano, Maria Giuseppina; Annual Meeting of the Neapolitan Brain Group 8. <2018 ; Naples> |
| 2019 | P27. The smallest 7Q11.23 duplication encompassing GTF2I and GTF2IRD1 genes in an individual with intellectual disability | Pinelli, Michele; Terrone, Gaetano; Cappuccio, Gerarda; Imperati, Floriana; Pignataro, Piero; Merla, Giuseppe; Genesio, Rita; Del Giudice, Ennio; Brunetti-Pierri, Nicola; Annual Meeting of the Neapolitan Brain Group 8. <2018 ; Naples> |
| 2019 | P38. Corpus callosum abnormalities and autism spectrum disorders | Vitiello, Giuseppina; Imperati, Floriana G.; Terrone, Gaetano; Romaniello, Romina; D’Amico, Alessandra; Genesio, Rita; Severino, Mariasavina; The Italian CCA Study Group; Nitsch, Lucio; Borgatti, Renato; Riccio, Maria Pia; Bravaccio, Carmela; Del Giudice, Ennio; Annual Meeting of the Neapolitan Brain Group 8. <2018 ; Naples> |
| 2019 | P33. A case of developmental encephalopathy caused by a de novo KCNB1 gene mutation | Terrone, Gaetano; Romano, Adele; Gennaro, Elena; Taglialatela, Maurizio; Del Giudice, Ennio; Annual Meeting of the Neapolitan Brain Group 8. <2018 ; Naples> |