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SCREEN4CARE | Shortening the path to rare disease diagnosis by using newborn genetic screening and digital technologies

01-10-2021

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30-09-2026

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EU-Programme-Call
Horizon 2020
H2020-EU.3. SOCIETAL CHALLENGES
H2020-EU.3.1. SOCIETAL CHALLENGES - Health, demographic change and well-being
H2020-EU.3.1.0. Cross-cutting call topics
H2020-JTI-IMI2-2020-23-two-stage
IMI2-2020-23-05 Shortening the path to Rare Disease diagnosis by using newborn genetic screening and digital technologies
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