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 2 (2006), Issue 7 (July)

1. A cryptic full mutation in a male with a classical fragile X phenotype.
   Clin Genet, 70(1): 39-42. [Abstract] [Full-text]
2. Thermodynamics of the fragile X mental retardation protein RGG box interactions with G quartet forming RNA.
   Biochemistry, 45(27): 8319-30. [Abstract] [Full-text]
3. Local protein synthesis and spine morphogenesis: Fragile X syndrome and beyond.
   J Neurosci, 26(27): 7151-5. [Abstract] [Full-text]
4. Cyanotic episodes in a male child with fragile X syndrome.
   Dev Med Child Neurol, 48(8): 690-2. [Abstract] [Full-text]
5. Simplified molecular diagnosis of fragile X syndrome by fluorescent methylation-specific PCR and GeneScan analysis.
   Clin Chem, 52(8): 1492-500. [Abstract] [Full-text]
6. The fragile X mental retardation protein interacts with a distinct mRNA nuclear export factor NXF2.
   RNA, 12(8): 1446-9. [Abstract] [Full-text]

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