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

> **NCT07102966** · NA · RECRUITING · sponsor: **Baylor College of Medicine** · enrollment: 410 (estimated)

## Conditions studied

- Rare Diseases

## Interventions

- **GENETIC:** Rapid whole genome sequencing

## Key facts

- **NCT ID:** NCT07102966
- **Lead sponsor:** Baylor College of Medicine
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2025-10-28
- **Primary completion:** 2029-03-31
- **Final completion:** 2029-07-31
- **Target enrollment:** 410 (ESTIMATED)
- **Last updated:** 2026-01-27

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07102966

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07102966, "Genetic Study to Determine the Cause of Birth Defects in Newborns in Texas". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT07102966. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*