[1]
|
Bear, M. F., Huber, K. M., & Warren, S. T. (2004). The mGluR theory of Fragile X mental retardation. Trends in Neuroscience, 27, 370- 377.
|
[2]
|
Beckel-Mitchener, A., & Greenough, W. T. (2004). Correlates across the structural, functional, and molecular phenotypes of Fragile X syndrome. Mental Retardation and Developmental Disabilities Research Reviews, 10, 53-59.
|
[3]
|
Brennan, F. X., Albeck, D. S., & Paylor, R. (2006). Fmr1 knockout mice are impaired in a leverpress escape/avoidance task. Genes, Brain and Behavior, 5, 467-471.
|
[4]
|
Brown, W. T. (2002). The molecular biology of the fragile X mutation. In R. J. Hagerman, & P. J. Hagerman (Eds.), Fragile X syndrome: Diagnosis, treatment, and research (3rd ed., pp. 110-135). Baltimore, MD: The Johns Hopkins University Press.
|
[5]
|
D?len, G., & Bear, M. F. (2009). Fragile x syndrome and autism: From disease model to therapeutic targets. Journal of Neurodevelopmental Disorders, 1, 133-140.
|
[6]
|
Dutch-Belgian Fragile X Consortium. (1994). Fmr1 knockout mice: A model to study fragile X mental retardation. Cell, 78, 23-33.
|
[7]
|
Hagerman, R. J. (2002). The physical and behavioral phenotype. In R. J.
|
[8]
|
Hagerman, & P. J. Hagerman (Eds.), Fragile X syndrome: Diagnosis, treatment, and research (3rd ed., pp. 3-109). Baltimore, MD: The Johns Hopkins University Press.
|
[9]
|
Hessl, D., Glaser, B., Dyer-Friedman, J., & Reiss, A. L. (2006). Social behavior and cortisol reactivity in children with fragile X syndrome. Journal of Child Psychology and Psychiatry, 47, 602-610.
|
[10]
|
Irwin, S. A., Galvez, R., & Greenough, W. T. (2000). Dendritic spine abnormalities in fragile-X mental retardation syndrome. Cerebral Cortex, 10, 1038-1044.
|
[11]
|
Iwata, B. A., Pace, G. M., Dorsey, M. F., Zarcone, J. R., Vollmer, T. R., Smith, R. G., et al. (1994). The functions of self-injurious behavior: An experimental-epidemiological analysis. Journal of Applied Behavior Analysis, 27, 215-240.
|
[12]
|
Kau, A. S., Reider, E. E., Payne, L., Meyer, W. A., & Freund, L. (2000). Early behavior signs of psychiatric phenotypes in fragile X syndrome. American Journal on Mental Retardation, 105, 266-299.
|
[13]
|
McKinney, B. C., Grossman, A. W., Elisseou, N. M., & Greenough, W. T. (2005). Dendritic spine abnormalities in the occipital cortex of C57BL/6 fmr1 knockout mice. American Journal of Medical Genetics, Part B, 136, 98-102.
|
[14]
|
Miller, L. J., McIntosh, D. N., McGarth J., Shyu, V., Lampe, M., Taylor, A. K., et al. (1999). Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary report. American Journal of Medical Genetics, 183, 268-279.
|
[15]
|
Qin, M., Kang, J., & Smith, C. B. (2005). A null mutation for Fmr1 in female mice: Effects on regional cerebral metabolic rate for glucose and relationship to behavior. Neuroscience, 135, 999-1009.
|
[16]
|
Sherman, S. (2002). Epidemiology. In R. J. Hagerman, & P. J. Hagerman (Eds.), Fragile X syndrome: Diagnosis, treatment, and research (3rd ed., pp. 136-168). Baltimore, MD: The Johns Hopkins University Press.
|
[17]
|
Symons, F. J., Clark, R. D., Hatton, D. D., Skinner, M., & Bailey Jr., D. B. (2003). Self-injurious behavior in young boys with fragile X syndrome. American Journal of Medical Genetics, 118, 115-121.
|
[18]
|
Valdovinos, M. G., Parsa, R. A., & Alexander, M. L. (2009). Results of a nation-wide survey evaluating the side effects of psychotropic medication use in Fragile X syndrome. Journal of Developmental and Physical Disabilities, 21, 23-37.
|