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No reason yet to ch ange diagnostic criteria for Noonan, Costello and cardio-facio-cutaneous syndromes.
2008 Neri, Giovanni; Allanson, J; Kavamura, I.
No reason yet to change diagnostic criteria for Noonan, Costello and cardio-facio-cutaneous syndromes.
2008 Neri, Giovanni; Allanson, J; Kavamura, Mi
Non-fatherhood or mutation? A probabilistic approach to parental exclusion in paternity testing
2001 Dawid, A. P.; Mortera, J.; Pascali, Vincenzo Lorenzo
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
2012 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
The nutrigenomic investigation of C57BL/6N mice fed a short-term high-fat diet highlights early changes in clock genes expression
2013 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
On the nosology and pathogenesis of Wolf-Hirschhorn sindrome: genotype-phenotype correlation analysis of 80 patients and literature review.
2008 Zollino, Marcella; Murdolo, Marina; Marangi, Giuseppe; Pecile, V; Galasso, C; Mazzanti, L; Neri, Giovanni
Opportunities, Risks, and Limitations of Genetic Testing: Looking to the Future From Patients' Point of View
2015 Bertolotti, Mauro Maria
Oral-facial-digital syndromes: review and diagnostic guidelines
2007 Gurrieri, Fiorella; Franco, B.; Toriello, H.; Neri, Giovanni
Overlapping Clinical Manifestations with Costello Syndrome
2007 Narumi, Y.; Aoki, Y.; Neri, Giovanni; Niihori, T.; Matsubara, Y.
Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe
2021 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
Overview on molecular studies in olive (Olea europaea L.) : DNA markers application and first results in genome analysis.
2011 Bracci, Tania; Busconi, Matteo; Fogher, Corrado; Sebastiani, Luca
Partial epilepsy complicated by convulsive and non convulsive episodes of status epilepticus in a patient with ring chromosome 14 syndrome
2010 Giovannini, Silvia; Frattini, D; Scarano, A; Fusco, C; Bertani, G; Della Giustina, E; Martinelli, P; Orteschi, Daniela; Zollino, Marcella; Neri, Giovanni; Gobbi, G.
Paternity testing commission of the international society of forensic genetics. Recommendation on genetic investigations in paternity cases
2003 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
Paternity Testing Commission of the International Society of Forensic Genetics: recommendations on genetic investigations in paternity cases.
2002 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
Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13
1999 Gurrieri, Fiorella; Battaglia, A; Torrisi, L; Tancredi, R; Cavallaro, C; Sangiorgi, Eugenio; Neri, Giovanni
Phylogenetic evidence for multiple independent duplication events at the DYS19 locus
2007 Capelli, Cristian; Brisighelli, Francesca; Scarnicci, Francesca; Blanco Verea, A; Brion, M; Pascali, Vincenzo Lorenzo
Polymorphisms of the IgH enhancer HS1.2 and risk of systemic lupus erythematosus
2012 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
Population structure in the Mediterranean basin: A Y chromosome perspective
2006 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.
Preliminary data on cellulase encoding genes in the xylophagous beetle, Hylotrupes bajulus (Linnaeus)
2014 Busconi, Matteo; Berzolla, Alessia; Chiappini, Elisabetta
Probabilistic expert systems for forensic inference from genetic markers
2002 Dawid, A. P.; Mortera, J.; Pascali, Vincenzo Lorenzo; Van Boxel, D.
Data di pubblicazione | Titolo | Autore(i) | File |
---|---|---|---|
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 | |
1-gen-2002 | Probabilistic expert systems for forensic inference from genetic markers | Dawid, A. P.; Mortera, J.; Pascali, Vincenzo Lorenzo; Van Boxel, D. |
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