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: 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: Titomanlio, L Della Casa, R Lecora, M Farina, V Sebastio, G Andria, G Parenti, G

Citation: L. Titomanlio et al., Geleophysic dysplasia: 7-year follow-up study of a patient with an intermediate form, AM J MED G, 86(1), 1999, pp. 82-85

Authors: Sperandeo, MP Perone, L Di Micco, P Titomanlio, L Parenti, G Lecora, M Rizzolo, MG Andria, G

Citation: Mp. Sperandeo et al., A case of triploidy with prolonged survival: molecular demonstration of maternal origin of the extra haploid set, RIV ITAL P, 24(6), 1998, pp. 1142-1144