Scientists hunt hidden genetic clues in rare diseases
NCT ID NCT01087320
Summary
This study aims to discover the genetic causes of rare disorders like intellectual disabilities and birth anomalies that currently have no known genetic explanation. Researchers will use advanced genome sequencing technology to analyze DNA from about 2000 affected individuals and their family members. The goal is to improve diagnosis and understanding of these conditions, which could eventually lead to better treatments.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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National Institutes of Health Clinical Center
RECRUITINGBethesda, Maryland, 20892, United States
Conditions
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