Category: Newborn Screening
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This interview from the 2014 National PKU Alliance Conference shares information about a new resource for those in the newborn screening community.
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"For Katy" is now free to view thanks to PKULife.tv's sponsor, PKU Perspectives! Katy is seven years old and has Phenylketonuria (PKU), a rare genetic disease in which the body cannot metabolize protein properly. M...
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Rare Disease Day is an annual worldwide event with one goal in mind: to raise awareness of rare diseases. Please join us on the last day of February as we raise our voices to support those with rare diseases.
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The Story of Newborn Screening Presented by Association of Public Health Laboratories A Creative Control Films production
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