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Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness.
Sinibaldi, Lorenzo; Garone, Giacomo; Mandarino, Alessandra; Iarossi, Giancarlo; Chioma, Laura; Dentici, Maria Lisa; Merla, Giuseppe; Agolini, Emanuele; Micalizzi, Alessia; Mancini, Cecilia; Niceta, Marcello; Macchiaiolo, Marina; Diodato, Daria; Onesimo, Roberta; Blandino, Rita; Delogu, Angelica Bibiana; De Rosa, Gabriella; Trevisan, Valentina; Iademarco, Mariella; Zampino, Giuseppe; Tartaglia, Marco; Novelli, Antonio; Bartuli, Andrea; Digilio, Maria Cristina; Calcagni, Giulio.
  • Sinibaldi L; Medical Genetics Unit, IRCCS Bambino Gesù Children Hospital, Rome, Italy.
  • Garone G; Clinical and Experimental Neurology, IRCCS Bambino Gesù Children Hospital, Rome, Italy.
  • Mandarino A; Department of Neuroscience, Mental Health and Sensory Organs (NESMOS), Faculty of Medicine and Psychology, Sapienza University of Rome, Rome, Italy.
  • Iarossi G; Child and Adolescent Neuropsychiatry Unit, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
  • Chioma L; Department of Ophthalmology, IRCCS Bambino Gesù Children Hospital, Rome, Italy.
  • Dentici ML; Endocrinology and Diabetology Unit, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
  • Merla G; Medical Genetics Unit, IRCCS Bambino Gesù Children Hospital, Rome, Italy.
  • Agolini E; Laboratory of Regulatory & Functional Genomics, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Foggia, Italy.
  • Micalizzi A; Department of Molecular Medicine & Medical Biotechnology, University of Naples Federico II, Naples, Italy.
  • Mancini C; Laboratory of Medical Genetics, Translational Cytogenomics Research Unity, IRCCS Bambino Gesù Children Hospital, Rome, Italy.
  • Niceta M; Laboratory of Medical Genetics, Translational Cytogenomics Research Unity, IRCCS Bambino Gesù Children Hospital, Rome, Italy.
  • Macchiaiolo M; Molecular Genetics and Functional Genomics, IRCCS Bambino Gesù Children Hospital, Rome, Italy.
  • Diodato D; Molecular Genetics and Functional Genomics, IRCCS Bambino Gesù Children Hospital, Rome, Italy.
  • Onesimo R; Rare Diseases and Medical Genetics Unit, IRCCS Bambino Gesù Children Hospital, Rome, Italy.
  • Blandino R; Neuromuscular and Neurodegenerative Disorders Unit, IRCCS Bambino Gesù Children Hospital, Rome, Italy.
  • Delogu AB; Rare Diseases Unit, IRCCS Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.
  • De Rosa G; Pediatric Unit, IRCCS Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.
  • Trevisan V; Pediatric Unit, IRCCS Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.
  • Iademarco M; Pediatric Unit, IRCCS Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.
  • Zampino G; Pediatric Unit, IRCCS Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.
  • Tartaglia M; Rare Diseases Unit, IRCCS Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.
  • Novelli A; Rare Diseases Unit, IRCCS Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.
  • Bartuli A; Rare Diseases Unit, IRCCS Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.
  • Digilio MC; Pediatric Unit, IRCCS Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.
  • Calcagni G; Dipartimento Universitario Scienze della Vita e Sanità Pubblica, Università Cattolica Sacro Cuore, Rome, Italy.
Clin Genet ; 104(5): 528-541, 2023 11.
Article en En | MEDLINE | ID: mdl-37455656
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastornos del Neurodesarrollo / Cardiopatías Congénitas / Discapacidad Intelectual Tipo de estudio: Diagnostic_studies Límite: Child / Humans Idioma: En Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastornos del Neurodesarrollo / Cardiopatías Congénitas / Discapacidad Intelectual Tipo de estudio: Diagnostic_studies Límite: Child / Humans Idioma: En Año: 2023 Tipo del documento: Article