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Emberger syndrome: A rare association with hearing loss.
Zawawi, Faisal; Sokolov, Meirav; Mawby, Thomas; Gordon, Karen A; Papsin, Blake C; Cushing, Sharon L.
Afiliação
  • Zawawi F; Department of Otolaryngology, Head and Neck Surgery, Hospital for Sick Children, Toronto, ON Canada; Department of Otolaryngology, Head and Neck Surgery, University of Toronto, Toronto, ON Canada.
  • Sokolov M; Department of Otolaryngology, Head and Neck Surgery, Hospital for Sick Children, Toronto, ON Canada; Department of Otolaryngology, Head and Neck Surgery, University of Toronto, Toronto, ON Canada; Archie's Cochlear Implant Laboratory, Hospital for Sick Children, Toronto, ON Canada.
  • Mawby T; Department of Otolaryngology, Head and Neck Surgery, Hospital for Sick Children, Toronto, ON Canada; Department of Otolaryngology, Head and Neck Surgery, University of Toronto, Toronto, ON Canada.
  • Gordon KA; Department of Otolaryngology, Head and Neck Surgery, University of Toronto, Toronto, ON Canada; Archie's Cochlear Implant Laboratory, Hospital for Sick Children, Toronto, ON Canada; Department of Communication Disorders, Hospital for Sick Children, Toronto, ON Canada.
  • Papsin BC; Department of Otolaryngology, Head and Neck Surgery, Hospital for Sick Children, Toronto, ON Canada; Department of Otolaryngology, Head and Neck Surgery, University of Toronto, Toronto, ON Canada; Archie's Cochlear Implant Laboratory, Hospital for Sick Children, Toronto, ON Canada.
  • Cushing SL; Department of Otolaryngology, Head and Neck Surgery, Hospital for Sick Children, Toronto, ON Canada; Department of Otolaryngology, Head and Neck Surgery, University of Toronto, Toronto, ON Canada; Archie's Cochlear Implant Laboratory, Hospital for Sick Children, Toronto, ON Canada. Electronic addres
Int J Pediatr Otorhinolaryngol ; 108: 82-84, 2018 May.
Article em En | MEDLINE | ID: mdl-29605372
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Fator de Transcrição GATA2 / Perda Auditiva Neurossensorial / Linfedema Tipo de estudo: Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Int J Pediatr Otorhinolaryngol Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Fator de Transcrição GATA2 / Perda Auditiva Neurossensorial / Linfedema Tipo de estudo: Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Int J Pediatr Otorhinolaryngol Ano de publicação: 2018 Tipo de documento: Article