Validation of Optical Genome Mapping for the Identification of Constitutional Genomic Variants in a Postnatal Cohort

Clinical trial NCT05295277 · UNKNOWN

Trial details

NCT number: NCT05295277
Sponsor: Bionano Genomics
Status: UNKNOWN
Study type: OBSERVATIONAL

Developmental Disability Intellectual Disability Autism Spectrum Disorder Congenital Anomaly Fragile X Syndrome Facioscapulohumeral Muscular Dystrophy 1

Start date: 2020-11-30
Primary completion: 2024-03-31
Enrollment: 1000

View on ClinicalTrials.gov

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