المؤلفون: Atzeri, F.

المصدر: Il Foro Italiano, 1903 Jan 01. 28, 111/112-121/122.

URL الوصول: https://www.jstor.org/stable/23105216

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المؤلفون: Verdura, C., Tebaldi, C., Atzeri, F., Colombo, R. R., Bianchi, R., Fusi, M., Girasole, A., Molini, V., Raimondi, C., Vernich, M., Martelli, A.

المصدر: Medical & Surgical Pediatrics / Pediatria Medica e Chirurgica; gen/feb2012, Vol. 34 Issue 1, p21-22, 2p

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المؤلفون: Isabella Vasta, Bruno Dallapiccola, Francesca Atzeri, Cinzia Neri, Marco Tartaglia, Francesca Pantaleoni, Angelica Bibiana Delogu, Cheryl Cytrynbaum, Giovanni Neri, Emma De Feo, Andrea Ballabio, Anna Sarkozy, Angelo Selicorni, Claudio Carta, Gilda Cobellis, Edgar A. Pogna, Bruce D. Gelb, Katherine A. Rauen, Rosanna Weksberg, Giuseppe Zampino

المساهمون: Zampino, Giuseppe, Pantaleoni, Francesca, Carta, Claudio, Cobellis, Gilda, Vasta, Isabella, Neri, Cinzia, Pogna, Edgar A, De Feo, Emma, Delogu, Angelica, Sarkozy, Anna, Atzeri, Francesca, Selicorni, Angelo, Rauen, Katherine A, Cytrynbaum, Cheryl S, Weksberg, Rosanna, Dallapiccola, Bruno, Ballabio, Andrea, Gelb, Bruce D, Neri, Giovanni, Tartaglia, Marco, Zampino, G, Pantaleoni, F, Carta, C, Cobellis, G, Vasta, I, Neri, C, Pogna, E. A., DE FEO, E, Delogu, A, Sarkozy, A, Atzeri, F, Selicorni, A, Rauen, K. A., Cytrynbaum, C. S., Weksberg, R, Dallapiccola, B, Gelb, B. D., Neri, G, Tartaglia, M.

مصطلحات موضوعية: Parents, Adult, Male, Models, Molecular, DNA Mutational Analysis, Mutation, Missense, Biology, Cardiofaciocutaneous syndrome, medicine.disease_cause, Germline, DNA Mutational Analysi, Germline mutation, Costello syndrome, Genetics, medicine, Humans, Missense mutation, Abnormalities, Multiple, HRAS de novo, HRAS, Genetic Testing, Genetics (clinical), Germ-Line Mutation, Mutation, Infant, Newborn, Infant, Genetic Variation, Syndrome, Middle Aged, medicine.disease, Genes, ra, Pedigree, Genes, ras, Phenotype, Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA, Parent, Child, Preschool, Noonan syndrome, Female, Human

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3f2bf0f7519fc10b5f700cf06d72c48
http://hdl.handle.net/11591/407171

المؤلفون: Angelo Selicorni, Lidia Larizza, Cristina Gervasini, Francesca Atzeri, L. Giordano, Federica Mottadelli, Francesca Faravelli, Maria Teresa Divizia, Paola Castronovo, Stefano Manzini, Patrizia Colapietro, Donatella Milani, Maria Francesca Bedeschi, Giovanni Neri, Angela Bentivegna, Maria L Giovannucci Uzielli

المساهمون: Bentivegna, A, Milani, D, Gervasini, C, Castronovo, P, Mottadelli, F, Manzini, S, Colapietro, P, Giordano, L, Atzeri, F, Divizia, M, Uzielli, M, Neri, G, Bedeschi, M, Faravelli, F, Selicorni, A, Larizza, L

المصدر: BMC Medical Genetics, Vol 7, Iss 1, p 77 (2006)
BMC Medical Genetics

مصطلحات موضوعية: Adult, Male, lcsh:Internal medicine, MED/03 - GENETICA MEDICA, Adolescent, lcsh:QH426-470, DNA Mutational Analysis, Molecular Sequence Data, Nuclear Localization Signals, medicine.disease_cause, Frameshift mutation, medicine, Genetics, Missense mutation, Humans, Point Mutation, Genetics(clinical), Amino Acid Sequence, CREB-binding protein, Child, lcsh:RC31-1245, Genetics (clinical), Sequence Deletion, Rubinstein-Taybi Syndrome, Mutation, Rubinstein–Taybi syndrome, biology, Point mutation, medicine.disease, Molecular biology, CREB-Binding Protein, Pedigree, lcsh:Genetics, Italy, Rubinstein–Taybi syndrome, CREB binding protein, Child, Preschool, biology.protein, Mutation testing, Female, Sequence Alignment, Congenital disorder, Research Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b85f6633761b1d94e3b1e8a03476d36a