Sfoglia per ???browse.type.metadata.subjectErc2011???  

Opzioni
Vai a: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Mostrati risultati da 103 a 122 di 168
Data di pubblicazione Titolo Autore(i) File
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
1-gen-2008 No reason yet to ch ange diagnostic criteria for Noonan, Costello and cardio-facio-cutaneous syndromes. Neri, Giovanni; Allanson, J; Kavamura, I.
1-gen-2008 No reason yet to change diagnostic criteria for Noonan, Costello and cardio-facio-cutaneous syndromes. Neri, Giovanni; Allanson, J; Kavamura, Mi
1-gen-2001 Non-fatherhood or mutation? A probabilistic approach to parental exclusion in paternity testing Dawid, A. P.; Mortera, J.; Pascali, Vincenzo Lorenzo
1-gen-2012 De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Heinzen, El; Swoboda, Kj; Hitomi, Y; Gurrieri, Fiorella; Tiziano, Francesco Danilo; Nicole, S; Fontaine, B; De Vries, B; Walley, Nm; Heavin, S; Panagiotakaki, E; Koelewijn, S; Kamphorst, J; Geilenkirchen, M; Pelzer, N; Laan, L; Haan, J; Ferrari, Mirella; Van Den Maagdenberg, A; Fiori, S; Abiusi, Emanuela; Di Pietro, Lorena; Sweney, Mt; Newcomb, Tm; Viollet, L; Huff, C; Jorde, Lb; Reyna, Sp; Murphy, Kj; Shianna, Kv; Gumbs, Ce; Little, L; Silver, K; Ptáček, Lj; Haan, J; Herke, S Gk; Whitelaw, Cm; Webb, D; Lynch, Bj; Uldall, P; King, Md; Scheffer, Ie; Neri, Giovanni; Arzimanoglou, A; Sisodiya, Sm; Mikati, Ma; Goldstein, Db
1-gen-2013 The nutrigenomic investigation of C57BL/6N mice fed a short-term high-fat diet highlights early changes in clock genes expression Lizier, Michela; Bomba, Lorenzo; Minuti, Andrea; Chegdani, Fatima; Capraro, Jessica; Tondelli, Barbara; Mazza, Raffaele; Callegari, Maria Luisa; Trevisi, Erminio; Rossi, Filippo; Ajmone Marsan, Paolo; Lucchini, Franco
1-gen-2008 On the nosology and pathogenesis of Wolf-Hirschhorn sindrome: genotype-phenotype correlation analysis of 80 patients and literature review. Zollino, Marcella; Murdolo, Marina; Marangi, Giuseppe; Pecile, V; Galasso, C; Mazzanti, L; Neri, Giovanni
1-gen-2015 Opportunities, Risks, and Limitations of Genetic Testing: Looking to the Future From Patients' Point of View Bertolotti, Mauro Maria
1-gen-2007 Oral-facial-digital syndromes: review and diagnostic guidelines Gurrieri, Fiorella; Franco, B.; Toriello, H.; Neri, Giovanni
1-gen-2007 Overlapping Clinical Manifestations with Costello Syndrome Narumi, Y.; Aoki, Y.; Neri, Giovanni; Niihori, T.; Matsubara, Y.
1-gen-2021 Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe Genuardi, Maurizio; David Humberto Marmolejo, 1; Mark Yu Zheng Wong, 2; Svetlana Bajalica-Lagercrantz, 3; Marc Tischkowitz, 2; Judith Balmaña, 4; extended ERN-GENTURIS Thematic Group, 3
1-gen-2011 Overview on molecular studies in olive (Olea europaea L.) : DNA markers application and first results in genome analysis. Bracci, Tania; Busconi, Matteo; Fogher, Corrado; Sebastiani, Luca
Mostrati risultati da 103 a 122 di 168
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile