Skip to content
VuFind
    • English
    • Deutsch
    • Español
    • Français
    • Italiano
    • 日本語
    • Nederlands
    • Português
    • Português (Brasil)
    • 中文(简体)
    • 中文(繁體)
    • Türkçe
    • עברית
    • Gaeilge
    • Cymraeg
    • Ελληνικά
    • Català
    • Euskara
    • Русский
    • Čeština
    • Suomi
    • Svenska
    • polski
    • Dansk
    • slovenščina
    • اللغة العربية
    • বাংলা
    • Galego
    • Tiếng Việt
    • Hrvatski
    • हिंदी
    • Հայերէն
    • Українська
    • Sámegiella
    • Монгол
Advanced
  • P382: Professionals’ perspecti...
  • Cite this
  • Text this
  • Email this
  • Print
  • Export Record
    • Export to RefWorks
    • Export to EndNoteWeb
    • Export to EndNote
  • Permanent link
P382: Professionals’ perspectives on the use of digital tools to support patient recontact in clinical genetics

P382: Professionals’ perspectives on the use of digital tools to support patient recontact in clinical genetics

Bibliographic Details
Main Authors: Guylaine D'Amours, Emma Reble, Vernie Aguda, Marc Clausen, Salma Shickh, Chloe Mighton, June Carroll, Jordan Lerner-Ellis, Tanya Nelson, Julie Richer, Kasmintan Schrader, Emily Seto, Serena Shastri-Estrada, Kevin Thorpe, Yvonne Bombard
Format: Article
Language:English
Published: Elsevier 2023-01-01
Series:Genetics in Medicine Open
Online Access:http://www.sciencedirect.com/science/article/pii/S2949774423004181
  • Holdings
  • Description
  • Similar Items
  • Staff View

Internet

http://www.sciencedirect.com/science/article/pii/S2949774423004181

Similar Items

  • From the patient to the population: Use of genomics for population screening
    by: Chloe Mighton, et al.
    Published: (2022-10-01)
  • P538: Curious but cautious: Patients’ preferences for all types of clinically actionable genomic incidental results
    by: Salma Shickh, et al.
    Published: (2024-01-01)
  • P397: Clinical utility of all types of medically relevant secondary findings: A systematic evidence review
    by: Chloe Mighton, et al.
    Published: (2023-01-01)
  • P409: Clinical utility of genomic sequencing for hereditary cancer syndromes: An observational chart review
    by: Salma Shickh, et al.
    Published: (2023-01-01)
  • Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery
    by: Christine Elser, et al.
    Published: (2022-04-01)

Search Options

  • Search History
  • Advanced Search

Find More

  • Browse the Catalog
  • Browse Alphabetically
  • Explore Channels
  • Course Reserves
  • New Items

Need Help?

  • Search Tips
  • Ask a Librarian
  • FAQs