Invisible Illness Awareness Week 2016: Our Voices Need to Be Heard
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Genetic Research

Discussion in 'Genetic Testing and SNPs' started by SeaShel, Jul 6, 2009.

  1. SeaShel

    SeaShel Senior Member

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    AZ
    FYI - just saw this and am afraid I'll forget about it as I'm trying to get hubby to airport, so am posting the link. If this is a repetition, pls forgive.

    https://www.23andme.com/researchrevolution/

    Not me/cfs specific, but may be of interest because of our variety of co-issues.
     
  2. Cort

    Cort Phoenix Rising Founder

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    Raleigh, NC
    That is really something. I've never seen anything like that. Don't have the participate but it sure would be interesting. Thanks for passing it on.
     
  3. Jody

    Jody Senior Member

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    Canada
    It does look interesting.

    SeaShel, do you know if it is restricted to American citizens?
     

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