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  Fragile X Society India unveils world’s first short film on FXS

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  “Listening to my patients”: Interview with Dr Alice Montanaro on her PhD research

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  FraXI Board of Advisors member Prof Claudia Bagni leads new study on FXS and smell

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  A Rare Invisible String

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  Sequence of neuropsychiatric symptoms for fragile X-associated tremor/ataxia syndrome (FXTAS) is different in females compared to males, new study finds 

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  Rare but Real: A family’s story of myths, stigma, and Fragile X Syndrome

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  “Transparent, collaborative, and hopeful”: Postdoctoral Researcher Kayla Smith on the world of FXS research

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  “Rarely talked about”: a new paper calling for the use of empathetic and kind language in describing rare conditions

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  Halvvejs i mål: #Running theXforFragileX

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  Vi præsenterer Fragile Xchange: En global digital platform for FXS-ressourcer støttet af Boston Scientific Foundation Europe

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