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Gómez-Rodríguez MJ, Morales-Conejo M, Arteche-López A, Sánchez-Calvín MT, Quesada-Espinosa JF, Gómez-Manjón I, Palma-Milla C, Lezana-Rosales JM, Pérez de la Fuente R, Martin-Ramos M-L, et al. Fragile X Syndrome Caused by Maternal Somatic Mosaicism of FMR1 Gene: Case Report and Literature Review. Genes. 2022; 13(9):1609. https://doi.org/10.3390/genes13091609

Gómez-Rodríguez, Maria Jose, Montserrat Morales-Conejo, Ana Arteche-López, Maria Teresa Sánchez-Calvín, Juan Francisco Quesada-Espinosa, Irene Gómez-Manjón, Carmen Palma-Milla, Jose Miguel Lezana-Rosales, Ruben Pérez de la Fuente, Maria-Luisa Martin-Ramos, and et al. 2022. "Fragile X Syndrome Caused by Maternal Somatic Mosaicism of FMR1 Gene: Case Report and Literature Review" Genes 13, no. 9: 1609. https://doi.org/10.3390/genes13091609

Gómez-Rodríguez, M. J., Morales-Conejo, M., Arteche-López, A., Sánchez-Calvín, M. T., Quesada-Espinosa, J. F., Gómez-Manjón, I., Palma-Milla, C., Lezana-Rosales, J. M., Pérez de la Fuente, R., Martin-Ramos, M.-L., Fernández-Guijarro, M., Moreno-García, M., & Alvarez-Mora, M. I. (2022). Fragile X Syndrome Caused by Maternal Somatic Mosaicism of FMR1 Gene: Case Report and Literature Review. Genes, 13(9), 1609. https://doi.org/10.3390/genes13091609