New study uses DNA sequencing to uncover causes of fetal abnormalities
NCT ID NCT06054230
First seen Apr 30, 2026 · Last updated May 14, 2026 · Updated 1 time
Summary
This study looks at how advanced genetic testing (exome or genome sequencing) can help find the cause of structural problems in unborn babies. Researchers will test samples from 500 pregnant women whose standard tests did not explain the baby's condition. The goal is to learn more about these conditions and how doctors and families use genetic information during pregnancy.
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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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Locations
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University of California, San Francisco
San Francisco, California, 94143, United States
Conditions
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