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Lights and Shadows in the Genetics of Syndromic and Non-Syndromic Hearing Loss in the Italian Population.
Morgan, Anna; Lenarduzzi, Stefania; Spedicati, Beatrice; Cattaruzzi, Elisabetta; Murru, Flora Maria; Pelliccione, Giulia; Mazzà, Daniela; Zollino, Marcella; Graziano, Claudio; Ambrosetti, Umberto; Seri, Marco; Faletra, Flavio; Girotto, Giorgia.
Afiliação
  • Morgan A; Institute for Maternal and Child Health-IRCCS "Burlo Garofolo", 34137 Trieste, Italy.
  • Lenarduzzi S; Institute for Maternal and Child Health-IRCCS "Burlo Garofolo", 34137 Trieste, Italy.
  • Spedicati B; Institute for Maternal and Child Health-IRCCS "Burlo Garofolo", 34137 Trieste, Italy.
  • Cattaruzzi E; Department of Medicine, Surgery and Health Sciences, University of Trieste, 34125 Trieste, Italy.
  • Murru FM; Institute for Maternal and Child Health-IRCCS "Burlo Garofolo", 34137 Trieste, Italy.
  • Pelliccione G; Institute for Maternal and Child Health-IRCCS "Burlo Garofolo", 34137 Trieste, Italy.
  • Mazzà D; Institute for Maternal and Child Health-IRCCS "Burlo Garofolo", 34137 Trieste, Italy.
  • Zollino M; Institute for Maternal and Child Health-IRCCS "Burlo Garofolo", 34137 Trieste, Italy.
  • Graziano C; Fondazione Policlinico Universitario A. Gemelli, IRCCS, UOC Genetica, 00168 Rome, Italy.
  • Ambrosetti U; Istituto di Medicina Genomica, Università Cattolica Sacro Cuore, 00168 Rome, Italy.
  • Seri M; Unit of Medical Genetics, S. Orsola-Malpighi Hospital, 40138 Bologna, Italy.
  • Faletra F; Audiology and audiophonology, University of Milano/Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, 20122 Milano, Italy.
  • Girotto G; Unit of Medical Genetics, S. Orsola-Malpighi Hospital, 40138 Bologna, Italy.
Genes (Basel) ; 11(11)2020 10 22.
Article em En | MEDLINE | ID: mdl-33105617
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas de Diagnóstico Molecular / Surdez Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas de Diagnóstico Molecular / Surdez Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article