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Sfoglia per ???browse.type.metadata.subjectErc2011???  LS2_1 - Genomics, comparative genomics, functional genomics

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Data di pubblicazione Titolo Autore(i) File
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
1-gen-2010 Partial epilepsy complicated by convulsive and non convulsive episodes of status epilepticus in a patient with ring chromosome 14 syndrome Giovannini, Silvia; Frattini, D; Scarano, A; Fusco, C; Bertani, G; Della Giustina, E; Martinelli, P; Orteschi, Daniela; Zollino, Marcella; Neri, Giovanni; Gobbi, G.
1-gen-2003 Paternity testing commission of the international society of forensic genetics. Recommendation on genetic investigations in paternity cases Morling, N.; Allen, R.; Carracedo, A.; Geada, H.; Guidet, F.; Hallenberg, C.; Martin, W.; Mayr, W. r.; Olaisen, B.; Pascali, Vincenzo Lorenzo; Schneider, P. m.; Paternity Testing Commission, International Society Of Forensic Genetics
1-gen-2002 Paternity Testing Commission of the International Society of Forensic Genetics: recommendations on genetic investigations in paternity cases. Morling, N.; Allen, R.; Carracedo, A.; Geada, H.; Guidet, F.; Hallenberg, C.; Martin, W.; Mayr, W. r.; Olaisen, B.; Pascali, Vincenzo Lorenzo; Schneider, P. m.; Paternity Testing Commission Of The International Society Of Forensic, Genetics
1-gen-1999 Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13 Gurrieri, Fiorella; Battaglia, A; Torrisi, L; Tancredi, R; Cavallaro, C; Sangiorgi, Eugenio; Neri, Giovanni
1-gen-2007 Phylogenetic evidence for multiple independent duplication events at the DYS19 locus Capelli, Cristian; Brisighelli, Francesca; Scarnicci, Francesca; Blanco Verea, A; Brion, M; Pascali, Vincenzo Lorenzo
1-gen-2012 Polymorphisms of the IgH enhancer HS1.2 and risk of systemic lupus erythematosus Frezza, D; Tolusso, Barbara; Giambra, V; Gremese, Elisa; Marchini, M; Nowik, M; Serone, E; D'Addabbo, P; Mattioli, C; Canestri, S; Petricca, L; D'Antona, G; Birshtein, Bk; Scorza, R; Ferraccioli, Gianfranco
1-gen-2006 Population structure in the Mediterranean basin: A Y chromosome perspective Capelli, Cristian; Redhead, N; Romano, V; Calì, F; Lefranc, G; Delague, V; Megarbane, A; Felice, A; Pascali, Vincenzo Lorenzo; Neophytou, P. I.; Poulli, Z.; Novelletto, A.; Malaspina, P.; Terrenato, L.; Berebbi, A.; Fellous, M.; Thomas, M. G.; Goldstein, D. B.
1-gen-2014 Preliminary data on cellulase encoding genes in the xylophagous beetle, Hylotrupes bajulus (Linnaeus) Busconi, Matteo; Berzolla, Alessia; Chiappini, Elisabetta
Mostrati risultati da 111 a 130 di 168
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