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Cri du chat syndrome and primary ciliary dyskinesia: a common genetic cause on chromosome 5p.
Shapiro, Adam J; Weck, Karen E; Chao, Kay C; Rosenfeld, Margaret; Nygren, Anders O H; Knowles, Michael R; Leigh, Margaret W; Zariwala, Maimoona A.
Afiliación
  • Shapiro AJ; Montreal Children's Hospital, McGill University, Quebec, Canada; Department of Pediatrics, University of North Carolina, Chapel Hill, NC.
  • Weck KE; Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, NC.
  • Chao KC; Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, NC.
  • Rosenfeld M; Seattle Children's Hospital and Department of Pediatrics, University of Washington School of Medicine, Seattle, WA.
  • Nygren AO; MRC-Holland, Amsterdam, The Netherlands.
  • Knowles MR; Department of Medicine, University of North Carolina, Chapel Hill, NC.
  • Leigh MW; Department of Pediatrics, University of North Carolina, Chapel Hill, NC.
  • Zariwala MA; Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, NC.
J Pediatr ; 165(4): 858-61, 2014 Oct.
Article en En | MEDLINE | ID: mdl-25066065
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 5 / Síndrome de Kartagener / Síndrome del Maullido del Gato / Mutación Tipo de estudio: Diagnostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: J Pediatr Año: 2014 Tipo del documento: Article País de afiliación: Nueva Caledonia
Texto completo
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PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 5 / Síndrome de Kartagener / Síndrome del Maullido del Gato / Mutación Tipo de estudio: Diagnostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: J Pediatr Año: 2014 Tipo del documento: Article País de afiliación: Nueva Caledonia