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The IRB waived consent for the study.
All patients provided written informed consent for the study procedures.
All patients gave their written consent for the study.
Study Design: Patients undergoing midtrimester genetic amniocentesis for routine indications gave consent for the study.
The data is not available for sharing due to the confidentiality clause included in the informed consent for the study.
Informed consent for the study protocol and all procedures has been obtained from all patients prior to inclusion.
All participants gave written informed consent for the study prior to the experiment.
A written informed consent for the study was obtained from each family prior to testing.
The Committee on Human Research at both study sites approved the protocol and written consent for the study.
All patients gave consent for the study.
Participants provided written consent for the study.
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