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Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
Tassone F, Protic D, Allen EG, Archibald AD, Baud A, Brown TW, Budimirovic DB, Cohen J, Dufour B, Eiges R, Elvassore N, Gabis LV, Grudzien SJ, Hall DA, Hessl D, Hogan A, Hunter JE, Jin P, Jiraanont P, Klusek J, Kooy RF, Kraan CM, Laterza C, Lee A, Lipworth K, Losh M, Loesch D, Lozano R, Mailick MR, Manolopoulos A, Martinez-Cerdeno V, McLennan Y, Miller RM, Montanaro FAM, Mosconi MW, Potter SN, Raspa M, Rivera SM, Shelly K, Todd PK, Tutak K, Wang JY, Wheeler A, Winarni TI, Zafarullah M, Hagerman RJ. Tassone F, et al. Among authors: zafarullah m. Cells. 2023 Sep 21;12(18):2330. doi: 10.3390/cells12182330. Cells. 2023. PMID: 37759552 Free PMC article. Review.
Molecular Biomarkers in Fragile X Syndrome.
Zafarullah M, Tassone F. Zafarullah M, et al. Brain Sci. 2019 Apr 27;9(5):96. doi: 10.3390/brainsci9050096. Brain Sci. 2019. PMID: 31035599 Free PMC article. Review.
De Novo Large Deletion Leading to Fragile X Syndrome.
Jiraanont P, Manor E, Tabatadze N, Zafarullah M, Mendoza G, Melikishvili G, Tassone F. Jiraanont P, et al. Among authors: zafarullah m. Front Genet. 2022 May 11;13:884424. doi: 10.3389/fgene.2022.884424. eCollection 2022. Front Genet. 2022. PMID: 35646065 Free PMC article.
80 results