Pioneering Informed Consent for Return of Research Results to Breast Cancer Patients Facing Barriers to Implementation of Genomic Medicine: The Kenyan BRCA1/2 Testing Experience Using Whole Exome Sequencing

INTRODUCTION: Obtaining informed consent from study participants and disseminating the findings responsibly is a key principle required for ethically conducted clinical and genetic research. Reports from African researchers providing feedback on insights gained during the return of whole exome seque...

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Detalles Bibliográficos
Autores principales: Torrorey-Sawe, Rispah, van der Merwe, Nicole, Mining, Simeon Kipkoech, Kotze, Maritha J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089032/
https://www.ncbi.nlm.nih.gov/pubmed/32231682
http://dx.doi.org/10.3389/fgene.2020.00170

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089032/
https://www.ncbi.nlm.nih.gov/pubmed/32231682
http://dx.doi.org/10.3389/fgene.2020.00170

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