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Investigating barriers to genetic counseling and germline mutation testing in women with suspected hereditary breast and ovarian cancer syndrome and Lynch syndrome.
Shaw, Josephine; Bulsara, Caroline; Cohen, Paul A; Gryta, Madeleine; Nichols, Cassandra B; Schofield, Lyn; O'Sullivan, Sarah; Pachter, Nicholas; Hardcastle, Sarah J.
Afiliación
  • Shaw J; St. John of God Subiaco Hospital, Subiaco, Western Australia, Australia.
  • Bulsara C; Institute for Health Research, University of Notre Dame Australia, Fremantle, Western Australia, Australia.
  • Cohen PA; St. John of God Subiaco Hospital, Subiaco, Western Australia, Australia; Institute for Health Research, University of Notre Dame Australia, Fremantle, Western Australia, Australia; Division of Women's and Infants' Health, School of Medicine, University of Western Australia, Crawley, Western Australi
  • Gryta M; School of Medicine, University of Notre Dame Australia, Fremantle, Western Australia, Australia.
  • Nichols CB; Genetic Services of Western Australia, Subiaco, Western Australia, Australia; Inherited Cancer Connect Partnership (ICCon).
  • Schofield L; Genetic Services of Western Australia, Subiaco, Western Australia, Australia.
  • O'Sullivan S; Genetic Services of Western Australia, Subiaco, Western Australia, Australia; WOMEN Centre, West Leederville, Western Australia, Australia.
  • Pachter N; Genetic Services of Western Australia, Subiaco, Western Australia, Australia; School of Paediatrics and Child Health, University of Western Australia, Australia; School of Medicine and Pharmacology, University of Western Australia, Australia.
  • Hardcastle SJ; Health Psychology and Behavioural Medicine Research Group, School of Psychology and Speech Pathology, Faculty of Health Sciences, Curtin University, Perth, WA, Australia.
Patient Educ Couns ; 101(5): 938-944, 2018 05.
Article en En | MEDLINE | ID: mdl-29273311
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Neoplasias Colorrectales Hereditarias sin Poliposis / Pruebas Genéticas / Conocimientos, Actitudes y Práctica en Salud / Mutación de Línea Germinal / Síndrome de Cáncer de Mama y Ovario Hereditario / Asesoramiento Genético / Tamización de Portadores Genéticos Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Patient Educ Couns Año: 2018 Tipo del documento: Article País de afiliación: Australia
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Neoplasias Colorrectales Hereditarias sin Poliposis / Pruebas Genéticas / Conocimientos, Actitudes y Práctica en Salud / Mutación de Línea Germinal / Síndrome de Cáncer de Mama y Ovario Hereditario / Asesoramiento Genético / Tamización de Portadores Genéticos Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Patient Educ Couns Año: 2018 Tipo del documento: Article País de afiliación: Australia