A New Outlook: How Carrier Screening Shaped One Family’s Future
Myriad Genetics
FEBRUARY 21, 2024
Ashley’s journey to a diagnosis for Christopher probably felt like forever to their family. From symptom onset until diagnosis, searching families visit an average of more than seven specialists and spend 4.8 1 , 1–15 (2013). But in the world of rare genetic diseases, it was relatively short. years getting answers.
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