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Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment.
Rolf, Bradley A; Schneider, Jennifer L; Amendola, Laura M; Davis, James V; Mittendorf, Kathleen F; Schmidt, Mark A; Jarvik, Gail P; Wilfond, Benjamin S; Goddard, Katrina A B; Ezzell Hunter, Jessica.
Afiliación
  • Rolf BA; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, WA, USA.
  • Schneider JL; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Amendola LM; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, WA, USA.
  • Davis JV; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Mittendorf KF; Department of Translational and Applied Genomics, Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Schmidt MA; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Jarvik GP; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, WA, USA.
  • Wilfond BS; Treuman Katz Center for Pediatric Bioethics, Seattle Children's Hospital and Research Institute, Seattle, WA, USA.
  • Goddard KAB; Department of Pediatrics, University of Washington School of Medicine, Seattle, WA, USA.
  • Ezzell Hunter J; Department of Translational and Applied Genomics, Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
J Genet Couns ; 31(1): 230-241, 2022 02.
Article en En | MEDLINE | ID: mdl-34302314
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Homosexualidad Femenina / Minorías Sexuales y de Género / Neoplasias Tipo de estudio: Etiology_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Límite: Female / Humans Idioma: En Revista: J Genet Couns Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Homosexualidad Femenina / Minorías Sexuales y de Género / Neoplasias Tipo de estudio: Etiology_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Límite: Female / Humans Idioma: En Revista: J Genet Couns Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos