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Home Page - FD/MAS Patient Registry

FD/MAS Patient Registry registry powered by NORD platform.

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FD/MAS Patient Registry registry powered by NORD platform.
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Home Page - FD/MAS Patient Registry | fdmasregistry.org Reviews

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FD/MAS Patient Registry registry powered by NORD platform.

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News - FD/MAS Patient Registry

https://www.fdmasregistry.org/News

Welcome to the FD/MAS Patient Registry. Written by: Deanna Portero. Last update by: Deanna Portero. First posted: 10/31/2016 5:41:43 PM. Last updated: 10/31/2016 5:44:00 PM. FD/MAS Patient Registry is Open for Enrollment. If you are a person living with FD/MAS, or are the legal guardian of a person living with FD/MAS, you can enroll is this study. For more information about the study or how to enroll, please visit the About page for patients. Subscribe to the FDF newsletter.

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About FD/MAS Patient Registry - FD/MAS Patient Registry

https://www.fdmasregistry.org/Home/About

About FD/MAS Patient Registry. About FD/MAS Patient Registry. The FD/MAS Patient Registry is a research project that allows patients and families to share their experiences with fibrous dysplasia/McCune-Albright syndrome (FD/MAS) by completing a series of surveys. The surveys were created in collaboration with patients, parents, clinicians and researchers, so that the data can be used to answer some of the most important questions about FD/MAS, including:. How and when diagnoses are made,. Participation ...

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