20,000
Participants
Start Date
December 3, 2024
Primary Completion Date
December 31, 2025
Study Completion Date
December 31, 2025
newborn genetic screening and whole genome sequencing
newborn genetic screening (panel of treatable diseases); whole genome sequencing (if newborn develops symptoms suggestive of a genetic disease)
RECRUITING
Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Hôpital d'Enfants, Dijon
RECRUITING
Azienda Ospedaliero Universitaria di Modena, Neonatology Unit, Modena
RECRUITING
Unit Medical Genetics, Azienda Ospedaliero-Universitaria Sant'Anna, Ferrara
RECRUITING
Clinic for Neuropediatrics and Muscular Diseases, Freiburg University Medical Center, Freiburg im Breisgau
RECRUITING
Ospedale Pediatrivo Bambino Gesu IRCCS, Rome
RECRUITING
San Pietro Fatebenefratelli Hospital, Roma
Collaborators (1)
Innovative Medicines Initiative
OTHER
Università degli Studi di Ferrara
OTHER
Ospedale Pediatrico Bambin Gesù
OTHER
University of Siena
OTHER
Centre Hospitalier Universitaire Dijon
OTHER
Real Genix
UNKNOWN
University Hospital Goettingen
OTHER
Centro Nacional de Análisis Genómico
UNKNOWN
Genoox
UNKNOWN
Schwarzwald-Baar Clinic
UNKNOWN
Municipal Hospital Karlsruhe
UNKNOWN
University Hospital Freiburg
OTHER