Your browser doesn't support javascript.
loading
Proband-mediated interventions to increase disclosure of genetic risk in families with a BRCA or Lynch syndrome condition: a systematic review.
Young, Alison Luk; Imran, Aalya; Spoelma, Michael J; Williams, Rachel; Tucker, Katherine M; Halliday, Jane; Forrest, Laura E; Wakefield, Claire E; Butow, Phyllis N.
Afiliação
  • Young AL; School of Medicine and Public Health, The University of Newcastle, Callaghan, NSW, Australia. alison.young@newcastle.edu.au.
  • Imran A; Division of Obstetrics and Gynaecology, Royal North Shore Hospital, Sydney, NSW, Australia.
  • Spoelma MJ; Discipline of Psychiatry and Mental Health, School of Clinical Medicine, University of New South Wales, Sydney, NSW, Australia.
  • Williams R; Prince of Wales Clinical School, Faculty of Medicine, University of New South Wales, Randwick, NSW, Australia.
  • Tucker KM; Prince of Wales Hereditary Cancer Centre, Prince of Wales Hospital, Randwick, NSW, Australia.
  • Halliday J; Prince of Wales Clinical School, Faculty of Medicine, University of New South Wales, Randwick, NSW, Australia.
  • Forrest LE; Prince of Wales Hereditary Cancer Centre, Prince of Wales Hospital, Randwick, NSW, Australia.
  • Wakefield CE; Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Butow PN; Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
Eur J Hum Genet ; 31(1): 18-34, 2023 01.
Article em En | MEDLINE | ID: mdl-36253533
Assuntos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Revelação Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália País de publicação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Revelação Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália País de publicação: Reino Unido