First newborns join screening for 200 rare diseases The new study uses genome sequencing to detect more diseases earlier, when they can still be treated.
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2026. Április 22. Csilla, Noémi napja van
2026. Április 22. Csilla, Noémi napja van
First newborns join screening for 200 rare diseases The new study uses genome sequencing to detect more diseases earlier, when they can still be treated.
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