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- Check2 days agoChange DetectedThe website has updated the 'type of intervention' feature from version v2.13.3 to v2.14.0, indicating a significant change in its functionality.SummaryDifference0.2%
- Check9 days agoNo Change Detected
- Check17 days agoNo Change Detected
- Check24 days agoNo Change Detected
- Check31 days agoChange DetectedThe website has been updated from version v2.13.2 to v2.13.3.SummaryDifference0.1%
- Check38 days agoChange DetectedThe website has updated the contact details section for the study, clarifying that it now provides information for individuals who can answer questions about joining the study, along with the location details.SummaryDifference2%
- Check53 days agoChange DetectedThe website has added new features, while several detailed data fields and options for downloading study information in various formats have been removed.SummaryDifference4%
- Check60 days agoChange DetectedSeveral key resources related to phenylketonuria and genetic disorders have been removed, including links from MedlinePlus and Rare Diseases, which may impact access to important information on these topics.SummaryDifference0.5%
- Check67 days agoChange DetectedThe website has been updated to version 2.12.2, with new resources added related to phenylketonuria and inborn amino acid metabolism disorders, while the previous version 2.12.1 has been removed.SummaryDifference4%
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