Your browser doesn't support javascript.
loading
Using data from the 100,000 Genomes Project to resolve conflicting interpretations of a recurrent TUBB2A mutation.
Ragoussis, Vassilis; Pagnamenta, Alistair T; Haines, Rebecca L; Giacopuzzi, Edoardo; McClatchey, Martin A; Sampson, Julian R; Suri, Mohnish; Gardham, Alice; Cobben, Jan-Maarten; Osio, Deborah; Fry, Andrew E; Taylor, Jenny C.
Afiliación
  • Ragoussis V; Wellcome Centre for Human Genetics, Oxford University, Oxford, Oxfordshire, UK.
  • Pagnamenta AT; NIHR Biomedical Research Centre, Oxford, UK.
  • Haines RL; Wellcome Centre for Human Genetics, Oxford University, Oxford, Oxfordshire, UK alistair@well.ox.ac.uk.
  • Giacopuzzi E; NIHR Biomedical Research Centre, Oxford, UK.
  • McClatchey MA; East Midlands Regional Molecular Genetics Service, Nottingham University Hospitals NHS Trust, Nottingham, UK.
  • Sampson JR; Wellcome Centre for Human Genetics, Oxford University, Oxford, Oxfordshire, UK.
  • Suri M; NIHR Biomedical Research Centre, Oxford, UK.
  • Gardham A; Institute of Medical Genetics, University Hospital of Wales, Cardiff, UK.
  • Cobben JM; Division of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, UK.
  • Osio D; Institute of Medical Genetics, University Hospital of Wales, Cardiff, UK.
  • Fry AE; Division of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, UK.
  • Taylor JC; North West Thames Regional Genetics Service, Northwick Park Hospital, Harrow, London, UK.
J Med Genet ; 59(4): 366-369, 2022 04.
Article en En | MEDLINE | ID: mdl-33547136
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Tubulina (Proteína) Límite: Humans Idioma: En Revista: J Med Genet Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Tubulina (Proteína) Límite: Humans Idioma: En Revista: J Med Genet Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido