المؤلفون: Giuseppina Baldassarre, Luigi Tarani, Agostina De Crescenzo, Maria Vittoria Cubellis, Silvia Maitz, Maria Francesca Bedeschi, Margherita Silengo, Andrea Freschi, Marina Macchiaiolo, Cristina Molinatto, Silvia Russo, Donatella Milani, Luciano Calzari, Andrea Riccio, Milena Mariani, Giovanni Battista Ferrero, Andrea Bartuli, Lidia Larizza, Daniela Melis, Angelo Selicorni, Alessandro Mussa

المساهمون: A., Mussa, S., Russo, A. D., Crescenzo, A., Freschi, L., Calzari, S., Maitz, M., Macchiaiolo, C., Molinatto, G., Baldassarre, M., Mariani, L., Tarani, M. F., Bedeschi, D., Milani, D., Meli, A., Bartuli, Cubellis, MARIA VITTORIA, A., Selicorni, M. C., Silengo, L., Larizza, A., Riccio, G. B., Ferrero, Mussa, Alessandro, Russo, Silvia, de Crescenzo, Agostina, Freschi, Andrea, Calzari, Luciano, Maitz, Silvia, Macchiaiolo, Marina, Molinatto, Cristina, Baldassarre, Giuseppina, Mariani, Milena, Tarani, Luigi, Bedeschi, Maria Francesca, Milani, Donatella, Melis, Daniela, Bartuli, Andrea, Cubellis, Maria Vittoria, Selicorni, Angelo, Cirillo Silengo, Margherita, Larizza, Lidia, Riccio, Andrea, Ferrero, Giovanni Battista

المصدر: European journal of human genetics (Online) (2015). doi:10.1038/ejhg.2015.88
info:cnr-pdr/source/autori:Mussa A.; Russo S.; de Crescenzo A.; Freschi A.; Calzari L.; Maitz S.; Macchiaiolo M.; Molinatto C.; Baldassarre G.; Mariani M.; Tarani L.; Bedeschi M.F.; Milani D.; Melis D.; Bartuli A.; Cubellis M.V.; Selicorni A.; Cirillo Silengo M.; Larizza L.; Riccio A.; Ferrero G.B./titolo:(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome/doi:10.1038%2Fejhg.2015.88/rivista:European journal of human genetics (Online)/anno:2015/pagina_da:/pagina_a:/intervallo_pagine:/volume

مصطلحات موضوعية: Male, 0301 basic medicine, Hepatoblastoma, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Beckwith-Wiedemann Syndrome, Genotype, Beckwith–Wiedemann syndrome, genotype-phenotype correlation, 030105 genetics & heredity, Biology, Gastroenterology, Article, Chromosomes, Organomegaly, Genomic Imprinting, 03 medical and health sciences, paternal uniparental disonomy, assisted reproductive technology, Neoplasms, Internal medicine, Genetics, medicine, Macroglossia, Humans, Pair 11, Cyclin-Dependent Kinase Inhibitor p57, Genetic Association Studies, Genetics (clinical), Chromosomes, Human, Pair 11, Cytogenetics, DNA Methylation, Female, Phenotype, medicine.disease, Chromosomal region, Nevus flammeus, medicine.symptom, Human

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::077edba535dc3707e8803d0aa1796385
http://hdl.handle.net/11588/608470