The Belgian Genome Resource to Resolve Rare Diseases

NACompletedINTERVENTIONAL
Enrollment

567

Participants

Timeline

Start Date

June 2, 2021

Primary Completion Date

July 5, 2024

Study Completion Date

January 31, 2025

Conditions
Intellectual Developmental DisorderMalformationsDysmorphiaDevelopmental Delay (Disorder)
Interventions
DIAGNOSTIC_TEST

Whole exome sequencing

Whole exome sequencing using Illumina short read sequencing

DIAGNOSTIC_TEST

Whole genome Sequencing

Whole genome sequencing using Illumina short read sequencing

Trial Locations (1)

Unknown

KU Leuven, Leuven

All Listed Sponsors
collaborator

Universitair Ziekenhuis Brussel

OTHER

collaborator

Erasme University Hospital

OTHER

collaborator

University Ghent

OTHER

collaborator

Universiteit Antwerpen

OTHER

collaborator

Université de Liège

OTHER

collaborator

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

OTHER

collaborator

Institut de Pathologie et de Génétique Charleroi

OTHER

lead

Universitaire Ziekenhuizen KU Leuven

OTHER