The fragile X prevalence paradox

J Med Genet. 2008 Aug;45(8):498-9. doi: 10.1136/jmg.2008.059055. Epub 2008 Apr 15.
No abstract available

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Female
  • Fragile X Mental Retardation Protein / genetics
  • Fragile X Syndrome / epidemiology*
  • Fragile X Syndrome / genetics
  • Fragile X Syndrome / physiopathology
  • Gene Frequency
  • Humans
  • Male
  • Mutation
  • Prevalence
  • Sex Characteristics
  • Trinucleotide Repeats

Substances

  • FMR1 protein, human
  • Fragile X Mental Retardation Protein