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Data di pubblicazione Titolo Autore(i) File
1-gen-1998 International workshop on Capillary Electrophoresis in the Forensic Sciences, University of Verona, Italy, 29 August 1997: Foreward Tagliaro, F; Pascali, Vincenzo Lorenzo
1-gen-2007 ISFG: Recommendations on biostatistics in paternity testing Gjertson, Dw; Brenner, Ch; Baur, Mp; Carracedo, Angel; Guidet, F; Lugue, Ja; Lessig, R; Mayr, Wr; Pascali, Vincenzo Lorenzo; Schneider, Pm; Morling, N.
1-gen-2001 L-acetylcarnitine treatment on fragile X patients hyperactive behaviour Calvani, M; D'Iddio, S; De Gaetano, A; Mariotti, Paolo; Mosconi, Luigi; Pomponi, Maria Grazia; Tabolacci, Elisabetta; Torrioli, Maria Giulia; Vernacotola, Silvia; Neri, Giovanni
1-gen-2007 Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new case Garavelli, Livia; Guareschi, E; Errico, S; Simoni, A; Bergonzini, P; Zollino, Marcella; Gurrieri, Fiorella; Mancini, Gm; Schot, R; Van Der Spek, Pj; Frigieri, G; Zonari, P; Albertini, E; Giustina, Ed; Amarri, S; Bianchini, G; Dobyns, Wb; Neri, Giovanni
1-gen-2009 Metagenomics analysis of microbiota from fermented sausages before ripening Busconi, Matteo; Marudelli, Mariangela; Rossi, Dario; Fogher, Corrado
1-gen-2000 Microsatellite variation in Central Africa: an analysis of intrapopulational and interpopulational genetic diversity Destro Bisol, G; Boschi, Ilaria; Caglià, A; Tofanelli, S; Pascali, Vincenzo Lorenzo; Paoli, G; Spedini, G.
1-gen-2008 Modest reactivation of the mutatnt FMR1 gene by valproic acid is accompanied by histone modifications but not DNA demethylation. Tabolacci, Elisabetta; De Pascalis, Ivana; Accadia, Maria; Terracciano, Alessandra; Moscato, Umberto; Chiurazzi, Pietro; Neri, Giovanni
1-gen-2019 Molecular analysis and sport performance in élite rugby union players. Pasqualetti, Massimo; Canu, Giulia; Minazzato, L.; Urbani, Andrea; Mordente, Alvaro; Galvani, Christel
1-gen-2007 Molecular and clinical characterization of cardio-facio-cutaneous (CFC) syndrome: overlapping clinical manifestations with Costello syndrome. Narumi, Y.; Aoki, Y.; Niihori, T.; Neri, Giovanni; Cave', H.; Verloes, A.; Nava, C.; Kavamura, M. I.; Okamoto, N.; Kurosawa, K.; Hennekam, R. C. M.; Wilson, L. C.; Gillessen Kaesbach, G.; Wieczorek, D.; Lapunzina, P.; Ohashi, H.; Makita, Y.; Kondo, I.; Tsuchiya, S.; Ito, E.; Sameshima, K.; Kato, K.; Kure, S.; Matsubara, Y.
1-gen-2005 Molecular autopsy of sudden cardiac death (SCD): The challenge of forensic pathologist to the complexity of genomics Oliva, Antonio; Pascali, Vincenzo Lorenzo; Hong, K; Brugada, R.
1-gen-2014 Molecular Characterization of Citrus Cultivars: Insight from Recent Sudies Marocco, Adriano; Bernardi, Jamila; Caaruso, Paola; Licciardello, Concetta
1-gen-2012 Molecular marker analysis of the genetic variability inside the species Crocus sativus L. Busconi, Matteo; Sanchez, Rosana; Fernandez, Jose Antonio
1-gen-2012 Molecular Markers Analysis of the Genetic Variability inside the Species Crocus sativus L. Busconi, Matteo; Santaella, Marcela; Sanchez, Rosana; Roldan, Marta; Fernandez, Jose Antonio
1-gen-2011 Molecular studies in olive (Olea europaea L.): overview on DNA markers applications and recent advances in genome analysis. Bracci, Tania; Busconi, Matteo; Fogher, Corrado; Sebastiani, Luca
1-gen-2009 Morphology and immunophenotyping of a monolateral ovotestis in a 46,XderY/45,X mosaic individual with ambiguous genitalia Zannoni, G. F; Vellone, G; Cordisco, E. L; Sangiorgi, Eugenio; Grimaldi, Maria Eufemia; Neri, Caterina; Nanni, L; Neri, Giovanni
1-gen-2007 MRX87 family with Aristales Xdup24bp mutation and implication for polyAlanine expansions. Laperuta, C.; Spizzichino, Letizia; D'Adamo, P.; Monfregola, J.; Maiorino, A.; D'Eustacchio, A.; Ventruto, V.; Neri, Giovanni; D'Urso, M.; Chiurazzi, Pietro; Ursini, M. V.; Miano, M. . G.
1-gen-2009 Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome Neumann, Te; Allanson, J; Kavamura, I; Kerr, B; Neri, Giovanni; Noonan, J; Corderddu, V; Gibson, K; Tzschach, A; Kruger, G; Hoeltzenbein, M; Goecke, To; Kehl, Hg; Albrecht, B; Luczak, K; Sasiadek, Mm; Musante, L; Laurie, R; Peters, H; Tartaglia, Marco; Zenker, M; Kalscheuer, V.
1-gen-2012 Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype Zollino, Marcella; Orteschi, Daniela; Murdolo, Marina; Lattante, Serena; Battaglia, Domenica Immacolata; Stefanini, Maria Chiara; Mercuri, Eugenio Maria; Chiurazzi, Pietro; Neri, Giovanni; Marangi, Giuseppe
1-gen-2003 MYH9 spectrum of autosomal-dominant giant platelet syndromes: unexpected association with fibulin-1 variant-D inactivation Toren, A; Rozenfeld Granot, G; Heath, Ke; Amariglio, N; Rocca, Bianca; Crosson, J; Epstein, Cj; Laghi, F; Landolfi, Raffaele; Carlsson, Le; Argraves, S; Bizzaro, N; Moxey Mims, M; Brok Simoni, F; Martignetti, Ja; Greinacher, A; Rechavi, G.
1-gen-1992 New phenomenon of correlation between measurements errors pertaining to heterozygous DNA profiles Pascali, Vincenzo Lorenzo; D'Aloja, Ernesto; Dobosz, Marina
Mostrati risultati da 92 a 111 di 168
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