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Sporadic vestibular schwannoma: a molecular testing summary.
Sadler, Katherine V; Bowers, Naomi L; Hartley, Claire; Smith, Philip T; Tobi, Simon; Wallace, Andrew J; King, Andrew; Lloyd, Simon K W; Rutherford, Scott; Pathmanaban, Omar N; Hammerbeck-Ward, Charlotte; Freeman, Simon; Stapleton, Emma; Taylor, Amy; Shaw, Adam; Halliday, Dorothy; Smith, Miriam Jane; Evans, D Gareth.
Affiliation
  • Sadler KV; Manchester Centre for Genomic Medicine, The University of Manchester, Manchester, UK.
  • Bowers NL; Genetic Medicine, University of Manchester, Manchester, UK.
  • Hartley C; Genetic Medicine, Regional Genetic Laboratories, Manchester, UK.
  • Smith PT; Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Manchester, UK.
  • Tobi S; Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Manchester, UK.
  • Wallace AJ; Manchester University NHS Foundation Trust, Manchester, UK.
  • King A; Neurosurgery, Salford Royal Hospital, Manchester, UK.
  • Lloyd SKW; Department of Otolaryngology, Manchester Royal Infirmary, Manchester, UK.
  • Rutherford S; Neurosurgery, Salford Royal Hospital, Manchester, UK.
  • Pathmanaban ON; Department of Neurosurgery, Salford Royal NHS Foundation Trust, Salford, UK.
  • Hammerbeck-Ward C; Department of Neurosurgery, Salford Royal NHS Foundation Trust, Salford, UK.
  • Freeman S; ENT, Manchester Royal infirmary, Manchester, UK.
  • Stapleton E; Department of Otolaryngology, Manchester Royal Infirmary, Manchester, UK.
  • Taylor A; Clinical Genetics, East Anglian Medical Genetics Service, Cambridge, UK.
  • Shaw A; Department of Genetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Halliday D; Oxford Centre for Genetic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Smith MJ; Neurosciences, NF2 Unit, Oxford, UK.
  • Evans DG; Genetic Medicine, University of Manchester, Manchester, UK.
J Med Genet ; 58(4): 227-233, 2021 04.
Article de En | MEDLINE | ID: mdl-32576656
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Facteurs de transcription / Neurinome de l'acoustique / Neurofibromine-2 / Protéine SMARCB1 Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Langue: En Journal: J Med Genet Année: 2021 Type de document: Article Pays d'affiliation: Royaume-Uni
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Facteurs de transcription / Neurinome de l'acoustique / Neurofibromine-2 / Protéine SMARCB1 Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Langue: En Journal: J Med Genet Année: 2021 Type de document: Article Pays d'affiliation: Royaume-Uni