Genomic Study of Congenital Malformation
NCT01250613 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 900
Last updated 2010-12-01
Summary
Genomic aberrations in patients diagnosed as congenital malformation with unknown etiology will be identified using high-density oligonucleotide array.
Conditions
- Genomic Aberrations in Patients Diagnosed as Congenital Malformation With Unknown Etiology
Sponsors & Collaborators
-
Academia Sinica, Taiwan
collaborator OTHER -
China Medical University Hospital
lead OTHER
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-06-30
Countries
- Taiwan
Study Locations
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