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

Autor: Vafaeie F; Medical Genetics Laboratory, Genetic Foundation of Khorasan Razavi, Mashhad, IRN., Alerasool M; Medical Genetics Laboratory, Genetic Foundation of Khorasan Razavi, Mashhad, IRN.; Department of Medical Genetics, Mashhad University of Medical Sciences, Mashhad, IRN., Kaseb Mojaver N; Medical Genetics Laboratory, Genetic Foundation of Khorasan Razavi, Mashhad, IRN., Mojarrad M; Medical Genetics Laboratory, Genetic Foundation of Khorasan Razavi, Mashhad, IRN.; Department of Medical Genetics, Mashhad University of Medical Sciences, Mashhad, IRN.; Genetic Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, IRN.

Publikováno v: Cureus [Cureus] 2021 Jul 12; Vol. 13 (7), pp. e16340. Date of Electronic Publication: 2021 Jul 12 (Print Publication: 2021).