RecruitingNCT05436587
Mutations and Phenotypes of Unclassifiable Inherited Bone Marrow Failure Syndromes
Studying Rare developmental defect during embryogenesis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Sohag University
- Principal Investigator
- Mahmoud I Yousef, PhDFaculty of Medicine, Sohag University
- Intervention
- The whole-exome sequencing(genetic)
- Enrollment
- 250 target
- Eligibility
- All sexes
- Timeline
- 2022 – 2028
Study locations (1)
- , Faculty of Medicine, Sohag University, Sohag, Egypt
Collaborators
Kyoto University · Assiut University
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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