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Response to Prakash et al.
Tuke, Marcus A; Ruth, Katherine S; Wood, Andrew R; Beaumont, Robin N; Tyrrell, Jessica; Jones, Samuel E; Yaghootkar, Hanieh; Turner, Claire L S; Donohoe, Mollie E; Brooke, Antonia M; Collinson, Morag N; Freathy, Rachel M; Weedon, Michael N; Frayling, Timothy M; Murray, Anna.
Afiliación
  • Tuke MA; Genetics of Complex Traits, University of Exeter Medical School, Exeter, UK.
  • Ruth KS; Genetics of Complex Traits, University of Exeter Medical School, Exeter, UK.
  • Wood AR; Genetics of Complex Traits, University of Exeter Medical School, Exeter, UK.
  • Beaumont RN; Genetics of Complex Traits, University of Exeter Medical School, Exeter, UK.
  • Tyrrell J; Genetics of Complex Traits, University of Exeter Medical School, Exeter, UK.
  • Jones SE; Genetics of Complex Traits, University of Exeter Medical School, Exeter, UK.
  • Yaghootkar H; Genetics of Complex Traits, University of Exeter Medical School, Exeter, UK.
  • Turner CLS; Peninsula Clinical Genetics, Royal Devon & Exeter Hospital, Exeter, UK.
  • Donohoe ME; Macleod Diabetes & Endocrine Centre, Royal Devon & Exeter Hospital, Exeter, UK.
  • Brooke AM; Macleod Diabetes & Endocrine Centre, Royal Devon & Exeter Hospital, Exeter, UK.
  • Collinson MN; Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UK.
  • Freathy RM; Genetics of Complex Traits, University of Exeter Medical School, Exeter, UK.
  • Weedon MN; Genetics of Complex Traits, University of Exeter Medical School, Exeter, UK.
  • Frayling TM; Genetics of Complex Traits, University of Exeter Medical School, Exeter, UK.
  • Murray A; Genetics of Complex Traits, University of Exeter Medical School, Exeter, UK. A.Murray@exeter.ac.uk.
Genet Med ; 21(8): 1884-1885, 2019 08.
Article en En | MEDLINE | ID: mdl-30573795
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de Turner Límite: Adult / Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article
Texto completo
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XML
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de Turner Límite: Adult / Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article