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Genetic testing in motor neuron disease and frontotemporal dementia: a 5-year multicentre evaluation.
Cairns, Lauren M; Rankin, Julia; Hamad, Asma; Cooper, Nicola; Merrifield, Katrina; Jain, Vani; Rosser, Elisabeth; Rogers, Megan; Buston, Sarah; Stopford, Cheryl; Jones, Gabriela; Lefroy, Henrietta; Németh, Andrea H; Holden, Simon; Douglas, Andrew G L.
Afiliación
  • Cairns LM; Wessex Clinical Genetics Service, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Rankin J; Peninsula Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK.
  • Hamad A; Clinical Genetics Unit, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
  • Cooper N; Clinical Genetics Unit, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
  • Merrifield K; Clinical Genetics Unit, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
  • Jain V; All Wales Medical Genetics Service, University Hospital Wales, Cardiff, UK.
  • Rosser E; Clinical Genetics Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Rogers M; Bristol Regional Clinical Genetics Service, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Buston S; Bristol Regional Clinical Genetics Service, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Stopford C; Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Jones G; Clinical Genetics Service, Nottingham University Hospitals NHS Trust, Nottingham, UK.
  • Lefroy H; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Németh AH; Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, UK.
  • Holden S; Clinical Genetics, Addenbrooke's Treatment Centre, Cambridge, UK.
  • Douglas AGL; Wessex Clinical Genetics Service, University Hospital Southampton NHS Foundation Trust, Southampton, UK a.g.douglas@soton.ac.uk.
J Med Genet ; 59(6): 544-548, 2022 06.
Article en En | MEDLINE | ID: mdl-33963046
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de la Neurona Motora / Enfermedades Neurodegenerativas / Demencia Frontotemporal Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Límite: Humans Idioma: En Revista: J Med Genet Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de la Neurona Motora / Enfermedades Neurodegenerativas / Demencia Frontotemporal Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Límite: Humans Idioma: En Revista: J Med Genet Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido