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Otolaryngological features in a cohort of patients affected with 22q11.2 deletion syndrome: A monocentric survey.
Grasso, Fiorentino; Cirillo, Emilia; Quaremba, Giuseppe; Graziano, Vincenzo; Gallo, Vera; Cruoglio, Letizia; Botta, Carmine; Pignata, Claudio; Motta, Sergio.
Afiliação
  • Grasso F; Department of Translational Medical Sciences, Pediatric section, Federico II University, Naples, Italy.
  • Cirillo E; Department of Translational Medical Sciences, Pediatric section, Federico II University, Naples, Italy.
  • Quaremba G; Department of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
  • Graziano V; Department of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
  • Gallo V; Department of Translational Medical Sciences, Pediatric section, Federico II University, Naples, Italy.
  • Cruoglio L; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
  • Botta C; Department of Morphologic and Functional Diagnostics, Radiotherapy and Legal Medicine, Federico II University, Naples, Italy.
  • Pignata C; Department of Translational Medical Sciences, Pediatric section, Federico II University, Naples, Italy.
  • Motta S; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
Am J Med Genet A ; 176(10): 2128-2134, 2018 10.
Article em En | MEDLINE | ID: mdl-30207636
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Faringe / Fenótipo / Nariz / Síndrome de DiGeorge / Orelha Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Faringe / Fenótipo / Nariz / Síndrome de DiGeorge / Orelha Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália