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Type: Posts; User: Rima

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    Thank you Bill. We did a full/whole exome...

    Thank you Bill.
    We did a full/whole exome sequencing and they only found the heterogzyte F508del mutation.
    The CF sequencing for me revealed nothing, for my husband it revealed the same...
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    Advice about diagnosis please

    My 9 year old son is a carrier of F508del. We recently discovered this while trying to find out why he has had chronic diarrhea since the age of 2 years. He has never had any other symptoms of CF. ...
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