Your browser doesn't support javascript.
loading
Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access.
Amendola, Laura M; Shuster, Elizabeth; Leo, Michael C; Dorschner, Michael O; Rolf, Bradley A; Shirts, Brian H; Gilmore, Marian J; Okuyama, Sonia; Zepp, Jamilyn M; Kauffman, Tia L; Mittendorf, Kathleen F; Bellcross, Cecilia; Jenkins, Charisma L; Joseph, Galen; Riddle, Leslie; Syngal, Sapna; Ukaegbu, Chinedu; Goddard, Katrina A B; Wilfond, Benjamin S; Jarvik, Gail P.
Afiliação
  • Amendola LM; Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, WA. Electronic address: lauraa7@uw.edu.
  • Shuster E; Center for Health Research, Kaiser Permanente Northwest, Portland, OR.
  • Leo MC; Center for Health Research, Kaiser Permanente Northwest, Portland, OR.
  • Dorschner MO; Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, WA; Department of Laboratory Medicine and Pathology, UW Medicine, University of Washington, Seattle, WA.
  • Rolf BA; Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, WA.
  • Shirts BH; Department of Laboratory Medicine and Pathology, UW Medicine, University of Washington, Seattle, WA.
  • Gilmore MJ; Department of Translational and Applied Genomics (TAG), Center for Health Research, Kaiser Permanente Northwest, Portland, OR.
  • Okuyama S; Division of Hematology-Oncology, Denver Health and Hospital Authority, Denver, CO.
  • Zepp JM; Department of Translational and Applied Genomics (TAG), Center for Health Research, Kaiser Permanente Northwest, Portland, OR.
  • Kauffman TL; Center for Health Research, Kaiser Permanente Northwest, Portland, OR.
  • Mittendorf KF; Department of Translational and Applied Genomics (TAG), Center for Health Research, Kaiser Permanente Northwest, Portland, OR.
  • Bellcross C; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA.
  • Jenkins CL; Department of Translational and Applied Genomics (TAG), Center for Health Research, Kaiser Permanente Northwest, Portland, OR.
  • Joseph G; Department of Humanities and Social Sciences, University of California San Francisco, San Francisco, CA.
  • Riddle L; Department of Humanities and Social Sciences, University of California San Francisco, San Francisco, CA.
  • Syngal S; Division of Population Sciences, Dana-Farber Cancer Institute, Boston, MA; Division of Gastroenterology, Brigham and Women's Hospital, Boston, MA.
  • Ukaegbu C; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA.
  • Goddard KAB; Department of Translational and Applied Genomics (TAG), Center for Health Research, Kaiser Permanente Northwest, Portland, OR.
  • Wilfond BS; Treuman Katz Center for Pediatric Bioethics, Seattle Children's Hospital, Seattle, WA; Division of Bioethics and Paliative Care, Department of Pediatrics, University of Washington School of Medicine, Seattle, WA.
  • Jarvik GP; Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, WA.
Genet Med ; 24(6): 1196-1205, 2022 06.
Article em En | MEDLINE | ID: mdl-35305866
Assuntos
Palavras-chave
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 da Mama / Neoplasias do Colo Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Aspecto: Implementation_research Limite: Female / Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article
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 da Mama / Neoplasias do Colo Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Aspecto: Implementation_research Limite: Female / Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article