Massive study aims to give every baby a genetic health map
NCT ID NCT05990179
Summary
This study is testing whether a detailed genetic test can safely and effectively expand the list of rare diseases screened for in newborns. It will enroll 100,000 babies to see if finding these conditions early, even before symptoms appear, leads to better health outcomes. Parents can choose to participate and decide what kind of genetic health information they want to receive about their baby.
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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Columbia University Irving Medical Center/NYP
RECRUITINGNew York, New York, 10032, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
Conditions
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