Fragile X Syndrome Research Today is a free monthly online journal that collates and summarizes the latest research about Fragile X Syndrome, including details on symptoms, treatment, heritability, diagnosis.

Volume 3 (2007), Issue 8 (August)

1. Whole genome microarray analysis of gene expression in subjects with fragile X syndrome.
   Genet Med, 9(7): 464-72. [Abstract] [Full-text]
2. Contribution of social and information-processing factors to eye-gaze avoidance in fragile X syndrome.
   Am J Ment Retard, 112(5): 349-60. [Abstract] [Full-text]
3. Glioblastoma in a boy with fragile X: an unusual case of neuroprotection.
   Arch Dis Child, 92(9): 795-6. [Abstract] [Full-text]
4. The tetraplex (CGG)n destabilizing proteins hnRNP A2 and CBF-A enhance the in vivo translation of fragile X premutation mRNA.
   Nucleic Acids Res. [Abstract] [Full-text]
5. Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS).
   Neurology, 69(9): 851-9. [Abstract] [Full-text]

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