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Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients.
Boaretto, Francesca; Snijders, Deborah; Salvoro, Cecilia; Spalletta, Ambra; Mostacciuolo, Maria Luisa; Collura, Mirella; Cazzato, Salvatore; Girosi, Donatella; Silvestri, Michela; Rossi, Giovanni Arturo; Barbato, Angelo; Vazza, Giovanni.
Afiliación
  • Boaretto F; Department of Biology, University of Padova, Padova, Italy.
  • Snijders D; Department of Women's and Children's Health, University of Padova, Padova, Italy.
  • Salvoro C; Department of Biology, University of Padova, Padova, Italy.
  • Spalletta A; Department of Biology, University of Padova, Padova, Italy.
  • Mostacciuolo ML; Department of Biology, University of Padova, Padova, Italy.
  • Collura M; Cystic Fibrosis and Respiratory Pediatric Center, Arnas Children Hospital, Palermo, Italy.
  • Cazzato S; Department of Mother and Child Health, Salesi Children's Hospital, Ancona, Italy.
  • Girosi D; Pediatric Pulmonology Unit, Istitute Giannina Gaslini, Genova, Italy.
  • Silvestri M; Pediatric Pulmonology Unit, Istitute Giannina Gaslini, Genova, Italy.
  • Rossi GA; Pediatric Pulmonology Unit, Istitute Giannina Gaslini, Genova, Italy.
  • Barbato A; Department of Women's and Children's Health, University of Padova, Padova, Italy.
  • Vazza G; Department of Biology, University of Padova, Padova, Italy. Electronic address: giovanni.vazza@unipd.it.
J Mol Diagn ; 18(6): 912-922, 2016 11.
Article en En | MEDLINE | ID: mdl-27637300
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Kartagener / Predisposición Genética a la Enfermedad / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: J Mol Diagn Asunto de la revista: BIOLOGIA MOLECULAR Año: 2016 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos
Texto completo
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Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Kartagener / Predisposición Genética a la Enfermedad / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: J Mol Diagn Asunto de la revista: BIOLOGIA MOLECULAR Año: 2016 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos