Scientists search for hidden clues in DNA to solve mysterious fetal conditions
NCT ID NCT06475651
Summary
This study aims to understand the unique DNA patterns in fetuses with rare genetic diseases and birth defects. Researchers will analyze DNA samples from 63 participants, including fetuses and children, to see if these patterns differ from those found after birth. The goal is to gather knowledge that could one day help doctors diagnose these conditions earlier during pregnancy.
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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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Department of Genomic Medicine for Rare Diseases and the Multidisciplinary Center for Prenatal Diagnosis of the Necker-Enfants malades Hospital
RECRUITINGParis, 75015, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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