RAI1 GENE 17P11.2 DELETION+DUPLICATION

Clinical trials for RAI1 GENE 17P11.2 DELETION+DUPLICATION explained in plain language.

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Trials to join now! 1

Scientists hunt for clues to rare genetic disorders

Knowledge-focused Recruiting now

This observational study aims to find biological markers (biomarkers) for RAI1-related disorders, including Smith-Magenis and Potocki-Lupski syndromes. Researchers will study 90 participants through clinical exams, blood tests, optional skin biopsies, and sleep studies. The goal …

Matched conditions: RAI1 GENE 17P11.2 DELETION+DUPLICATION

Sponsor: Baylor College of Medicine • Aim: Knowledge-focused

Last updated Jun 27, 2026 13:00 UTC

RAI1 GENE 17P11.2 DELETION+DUPLICATION

Get alerted when new RAI1 GENE 17P11.2 DELETION+DUPLICATION trials appear

Scientists hunt for clues to rare genetic disorders