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Travel can feel overwhelming — especially when routines change, environments are different, and there is a lot of unexpected input happening around you. We pulled together some resources to support your trip to the 20th International Fragile X Conference in Louisville, KY, this July, but they can be adapted for any upcoming travel.
Mom's Night Out
‘Fishing for a Cureʼ Reels in Over $20,000 This Year!
12 mins read
Research Funding Opportunities from CDMRP/PRMRP for FY26
03 mins read
Update from Shionogi on EXPERIENCE Fragile X Clinical Trial
04 mins read
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We’re thrilled to spotlight a major new review article recently published in the New England Journal of Medicine (NEJM) – The Spectrum of Fragile X Disorders by Randi J. Hagerman and Paul J. Hagerman.
Valuable resources to share with your care team or anyone seeking a better understanding of the genetics of Fragile X, including the Fragile X premutation, and answer questions about genetic testing and genetic counseling.
The Fragile X Program provides services and referrals for children and young adults with FXS and FXD, including FXTAS and FXPOI.
This report, from Summer Scholar Marwa Zafarullah, is based on a study to help us better understand the impact of the CGG repeats on the different clinical premutation phenotypes and the molecular mechanisms behind the development of Fragile X-associated disorders.