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Fragile X Program

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 Division of Genetics
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The Fragile X Program provides an integrated, multidisciplinary approach to care for people with fragile X syndrome and their families.

Supported by FRAXA Research Foundation, our program includes team members from Genetics, Developmental Pediatrics, Occupational Therapy, Neurology, and other medical services.

By using the combined knowledge and expertise of these providers, as well as community educational and support services, we provide a management program that addresses the specific needs of fragile X syndrome families.

In the Spotlight
Updates on Clinical Research and Fragile X Syndrome
On Thursday, July 23rd, the Children's Hospital Boston Fragile X Program sponsored a talk about the current state of clinical research and fragile X syndrome. The talk was recorded and is now available for viewing by selecting the link above.
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Related topics:
Genetic Services
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