Authors: De Brasi, D Rossi, E Giglio, S D'Agostino, A Titomanlio, L Farina, V Andria, G Sebastio, G

Citation: D. De Brasi et al., Inv dup del (1)(pter -> q44 :: q44 -> q42 :) with the classical phenotype of trisomy 1q42-qter, AM J MED G, 104(2), 2001, pp. 127-130

Authors: Titomanlio, L Marzano, MG Rossi, E D'Armiento, M De Brasi, D Vega, GR Andreucci, MV Orsini, AVM Santoro, L Sebastio, G

Citation: L. Titomanlio et al., Case of Myhre syndrome with autism and peculiar skin histological findings, AM J MED G, 103(2), 2001, pp. 163-165

Authors: Feliciello, A Allevato, G Musti, AM De Brasi, D Gallo, A Avvedimento, VE Gottesman, ME

Citation: A. Feliciello et al., Thyroid transcription factor 1 phosphorylation is not required for proteinkinase A-dependent transcription of the thyroglobulin promoter, CELL GROWTH, 11(12), 2000, pp. 649-654

Authors: De Brasi, D Della Casa, R Titomanlio, L D'Agostino, A Perone, L Andria, G

Citation: D. De Brasi et al., Mental retardation, tall stature and minor phenotypic abnormalities associated with a de novo complex chromosome rearrangement, NEUROPEDIAT, 31(3), 2000, pp. 164-166

Authors: De Brasi, D Esposito, T Rossi, M Parenti, G Sperandeo, MP Zuppaldi, A Bardaro, T Ambruzzi, MA Zelante, L Ciccodicola, A Sebastio, G D'Urso, M Andria, G

Citation: D. De Brasi et al., Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of Delta7-sterol reductase in Italy and report of three novel mutations, EUR J HUM G, 7(8), 1999, pp. 937-940

Authors: De Brasi, D Berone, L Di Micco, P Andria, G Sebastio, G Iaccarino, E Pinto, L Aliberti, F

Citation: D. De Brasi et al., Cloverleaf skull anomaly and de novo trisomy 4p, J MED GENET, 36(5), 1999, pp. 422-424