Autonomy and the patient's right ‘not to know’ in clinical whole-genomic sequencing

Title

Autonomy and the patient's right ‘not to know’ in clinical whole-genomic sequencing

Creator

Townsend A; Rousseau F; Friedman J; Adam S; Lohn Z; Birch P

Publisher

European Journal Of Human Genetics

Date

2013

Description

2013

Rights

Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).

Type

Journal Article

Citation List Month

Backlog

URL Address

http://doi.org/10.1038/ejhg.2013.94

Citation

Townsend A; Rousseau F; Friedman J; Adam S; Lohn Z; Birch P, “Autonomy and the patient's right ‘not to know’ in clinical whole-genomic sequencing,” Pediatric Palliative Care Library, accessed April 20, 2025, https://pedpalascnetlibrary.omeka.net/items/show/14737.