Two new cases of fragile X syndrome without CGG triplet expansion. Clinical-molecular characterization and review of the literature

European Journal of Medical Genetics · Published 2026-07-15 · DOI 10.1016/j.ejmg.2026.105093

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Authors (12)

Giulia Lauretti, Roberta Pietrobono, Benedetta Niccolini, Clarissa Modafferi, Maria Accadia, Ada Piepoli, Daniela Orteschi, Maria Grazia Pomponi, Pietro Chiurazzi, Maurizio Genuardi, Giovanni Neri, Elisabetta Tabolacci

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Year

2026

Citation

Lauretti, G., Pietrobono, R., Niccolini, B., et al. (2026). Two new cases of fragile X syndrome without CGG triplet expansion. Clinical-molecular characterization and review of the literature. European Journal of Medical Genetics. https://doi.org/10.1016/j.ejmg.2026.105093

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