Skip to content
VuFind
Advanced
  • The risk of re-identification...
  • Cite this
  • Print
  • Export Record
    • Export to RefWorks
    • Export to EndNoteWeb
    • Export to EndNote
The risk of re-identification versus the need to identify individuals in rare disease research.
QR Code

The risk of re-identification versus the need to identify individuals in rare disease research.

Bibliographic Details
Main Authors: Hansson, M., Lochmuller, H., Riess, O., Schaefer, F., Orth, M., Rubinstein, Y., Molster, C., Dawkins, Hugh, Taruscio, D., Posada, M., Woods, S.
Format: Journal Article
Published: Nature Publishing Group 2016
Online Access:http://hdl.handle.net/20.500.11937/58552
  • Holdings
  • Description
  • Similar Items
  • Staff View

Internet

http://hdl.handle.net/20.500.11937/58552

Similar Items

  • International Charter of principles for sharing bio-specimens and data
    by: Mascalzoni, D., et al.
    Published: (2015)
  • Survey of healthcare experiences of Australian adults living with rare diseases.
    by: Molster, C., et al.
    Published: (2016)
  • Why we need international rare disease registers to study individual rare disorders associated with intellectual disabilities
    by: Leonard, H., et al.
    Published: (2016)
  • Role of international registries in enhancing the care of familial hypercholesterolaemia
    by: Hammond, E., et al.
    Published: (2013)
  • Indigenous genetics and rare diseases: Harmony, diversity and equity
    by: Baynam, Gareth, et al.
    Published: (2017)

Search Options

  • Advanced Search

Find More

  • Browse the Catalog

Need Help?

  • Search Tips