Scientists probe psychiatric secrets of rare genetic disorders
NCT ID NCT00768820
First seen May 01, 2026 · Last updated May 01, 2026
Summary
This study looks at how thinking, emotions, and behavior are affected in people with Velocardiofacial, Williams, or Fragile X syndrome. Researchers will use psychological tests and genetic analysis to find patterns. The goal is to better understand these conditions, not to test a new treatment. About 400 people with a confirmed genetic deletion or syndrome will take part.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Schneider Children's Mediac Center of Israel
RECRUITINGPetah Tikva, 49202, Israel
Contact Phone: •••-•••-••••
Conditions
Explore the condition pages connected to this study.