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RAI1 Gene 17P11.2 Deletion+Duplication

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RAI1 Gene 17P11.2 Deletion+Duplication

Explore clinical trials studying RAI1 Gene 17P11.2 Deletion+Duplication. Study availability and eligibility vary by location and protocol.

1 public trial 1 recruiting study

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RAI1 Gene 17P11.2 Deletion+Duplication trial results

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Clinical and Molecular Biomarker Studies in RAI1 (Retinoic Acid-Induced 1) -Related Disorders

NCT06274164

Conditions: Abnormalities, Multiple, Chromosome Disorders, Chronobiology Disorders, +7 more
Locations: Texas Children's Hospital Houston, Texas, United States

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