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Whole genome sequencing in the diagnosis of primary ciliary dyskinesia.
Wheway, Gabrielle; Thomas, N Simon; Carroll, Mary; Coles, Janice; Doherty, Regan; Goggin, Patricia; Green, Ben; Harris, Amanda; Hunt, David; Jackson, Claire L; Lord, Jenny; Mennella, Vito; Thompson, James; Walker, Woolf T; Lucas, Jane S.
Afiliación
  • Wheway G; School of Human Development and Health, Faculty of Medicine, University of Southampton, Southampton, UK. g.wheway@soton.ac.uk.
  • Thomas NS; Institute for Life Sciences, University of Southampton, Southampton, UK. g.wheway@soton.ac.uk.
  • Carroll M; School of Human Development and Health, Faculty of Medicine, University of Southampton, Southampton, UK.
  • Coles J; Wessex Regional Genetics Laboratory, Salisbury NSF Foundation Trust, Salisbury District Hospital, Salisbury, UK.
  • Doherty R; School of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
  • Goggin P; School of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
  • Green B; Primary Ciliary Dyskinesia Centre, NIHR Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Harris A; School of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
  • Hunt D; Primary Ciliary Dyskinesia Centre, NIHR Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Jackson CL; Biomedical Imaging Unit, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Mennella V; School of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
  • Thompson J; Primary Ciliary Dyskinesia Centre, NIHR Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Walker WT; Biomedical Imaging Unit, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Lucas JS; Queen Alexandra Hospital, Portsmouth Hospitals NHS Trust, Portsmouth, UK.
BMC Med Genomics ; 14(1): 234, 2021 09 23.
Article en En | MEDLINE | ID: mdl-34556108
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastornos de la Motilidad Ciliar Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: BMC Med Genomics Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastornos de la Motilidad Ciliar Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: BMC Med Genomics Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido