Identification of novel mutations in patients with Coffin-Lowry syndrome by a denaturing HPLC-based assay

Clin Chem. 2005 Dec;51(12):2356-8. doi: 10.1373/clinchem.2005.056036.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, High Pressure Liquid / methods*
  • Coffin-Lowry Syndrome / genetics*
  • DNA Mutational Analysis / methods*
  • Female
  • Humans
  • Male
  • Mutation / genetics*
  • Nucleic Acid Denaturation