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Genetics in Medicine: February 2022

 
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When? This feed was archived on June 29, 2022 03:03 (2+ y ago). Last successful fetch was on May 04, 2022 13:48 (2+ y ago)

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Manage episode 319446111 series 48487
Content provided by Elsevier. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Elsevier or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
February: Matchmaking is an increasingly important strategy to help link rare diseases to genetic variants. These tools allow clinicians and researchers to search across previously siloed databases, clinics, and laboratories and access data about the potential genetic underpinnings of undiagnosed rare diseases across international boundaries. But to date there hasn’t been much research on the user experience.
  continue reading

148 episodes

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Archived series ("Inactive feed" status)

When? This feed was archived on June 29, 2022 03:03 (2+ y ago). Last successful fetch was on May 04, 2022 13:48 (2+ y ago)

Why? Inactive feed status. Our servers were unable to retrieve a valid podcast feed for a sustained period.

What now? You might be able to find a more up-to-date version using the search function. This series will no longer be checked for updates. If you believe this to be in error, please check if the publisher's feed link below is valid and contact support to request the feed be restored or if you have any other concerns about this.

Manage episode 319446111 series 48487
Content provided by Elsevier. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Elsevier or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
February: Matchmaking is an increasingly important strategy to help link rare diseases to genetic variants. These tools allow clinicians and researchers to search across previously siloed databases, clinics, and laboratories and access data about the potential genetic underpinnings of undiagnosed rare diseases across international boundaries. But to date there hasn’t been much research on the user experience.
  continue reading

148 episodes

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