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Molecular marker analysis of the genetic variability inside the species Crocus sativus L.
2012 Busconi, Matteo; Sanchez, Rosana; Fernandez, Jose Antonio
Molecular Markers Analysis of the Genetic Variability inside the Species Crocus sativus L.
2012 Busconi, Matteo; Santaella, Marcela; Sanchez, Rosana; Roldan, Marta; Fernandez, Jose Antonio
Molecular studies in olive (Olea europaea L.): overview on DNA markers applications and recent advances in genome analysis.
2011 Bracci, Tania; Busconi, Matteo; Fogher, Corrado; Sebastiani, Luca
Morphology and immunophenotyping of a monolateral ovotestis in a 46,XderY/45,X mosaic individual with ambiguous genitalia
2009 Zannoni, G. F; Vellone, G; Cordisco, E. L; Sangiorgi, Eugenio; Grimaldi, Maria Eufemia; Neri, Caterina; Nanni, L; Neri, Giovanni
MRX87 family with Aristales Xdup24bp mutation and implication for polyAlanine expansions.
2007 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.
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome
2009 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.
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype
2012 Zollino, Marcella; Orteschi, Daniela; Murdolo, Marina; Lattante, Serena; Battaglia, Domenica Immacolata; Stefanini, Maria Chiara; Mercuri, Eugenio Maria; Chiurazzi, Pietro; Neri, Giovanni; Marangi, Giuseppe
MYH9 spectrum of autosomal-dominant giant platelet syndromes: unexpected association with fibulin-1 variant-D inactivation
2003 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.
New phenomenon of correlation between measurements errors pertaining to heterozygous DNA profiles
1992 Pascali, Vincenzo Lorenzo; D'Aloja, Ernesto; Dobosz, Marina
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
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 |
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