The FMR1 Phenotype: Premutation and Fragile X Syndrome
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Publisher
Springer Nature Switzerland
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-66932-3_14
Reference114 articles.
1. Abbeduto, L., Murphy, M. M., Kover, S. T., Giles, N. D., Karadottir, S., Amman, A., Bruno, L., Kim, J. S., Schroeder, S., Anderson, J. A., & Nollin, K. A. (2008). Signaling noncomprehension of language: A comparison of fragile X syndrome and Down syndrome. American Journal on Mental Retardation, 113(3). https://doi.org/10.1352/0895-8017(2008)113[214:SNOLAC]2.0.CO;2
2. Adams, P. E., Adams, J. S., Nguyen, D. V., Hessl, D., Brunberg, J. A., Tassone, F., Zhang, W., Koldewyn, K., Rivera, S. M., Grigsby, J., Zhang, L., DeCarli, C., Hagerman, P. J., & Hagerman, R. J. (2010). Psychological symptoms correlate with reduced hippocampal volume in fragile X premutation carriers. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 153(3), 775–785. https://doi.org/10.1002/ajmg.b.31046
3. Aishworiya, R., Protic, D., Tang, S. J., Schneider, A., Tassone, F., & Hagerman, R. (2022). Fragile X-associated neuropsychiatric disorders (FXAND) in young fragile X premutation carriers. Genes, 13(12). https://doi.org/10.3390/genes13122399
4. Allen, E. G., Sherman, S., Abramowitz, A., Leslie, M., Novak, G., Rusin, M., Scott, E., & Letz, R. (2005). Examination of the effect of the polymorphic CGG repeat in the FMR1 gene on cognitive performance. Behavior Genetics, 35(4), 435–445. https://doi.org/10.1007/s10519-005-2792-4
5. American Psychiatric Association. (2022). Diagnostic and statistical manual of mental disorders (5th ed., text rev.). https://doi.org/10.1176/appi.books.9780890425787
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