Fragile X Syndrome in a Female With Homozygous Full-Mutation Alleles of the FMR1 Gene

Farzane Vafaeie; Masoome Alerasool; Nasrin Kaseb Mojaver; Majid Mojarrad; Farzane Vafaeie; Masoume Ale Rasoul; Nasrin Kaseb Mojaver; Majid Mojarrad

doi:10.7759/cureus.16340

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