NCT07102966View on ClinicalTrials.gov

Genetic Study to Determine the Cause of Birth Defects in Newborns in Texas

NARecruitingINTERVENTIONAL
Enrollment

410

Participants

Timeline

Start Date

September 20, 2025

Primary Completion Date

March 31, 2029

Study Completion Date

July 31, 2029

Conditions
Rare Diseases
Interventions
GENETIC

Rapid whole genome sequencing

All consented patients will receive a virtual genetic evaluation and rapid whole genome sequencing

Trial Locations (1)

77030

RECRUITING

Baylor College of Medicine, Houston

All Listed Sponsors
collaborator

National Human Genome Research Institute (NHGRI)

NIH

lead

Baylor College of Medicine

OTHER

NCT07102966 - Genetic Study to Determine the Cause of Birth Defects in Newborns in Texas | Biotech Hunter | Biotech Hunter