Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative cases.

Lignende værker

• Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses.
  af: Philippe, C, et al.
  Udgivet: (1997)
• Breakpoint characterization of large deletions in <it>EXT1 </it>or <it>EXT2 </it>in 10 Multiple Osteochondromas families
  af: Szuhai Karoly, et al.
  Udgivet: (2011-06-01)
• Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostoses.
  af: Park, K, et al.
  Udgivet: (1999)
• Three Novel EXT1 and EXT2 Gene Mutations in Taiwanese Patients with Multiple Exostoses
  af: Wen-Chau Chen, et al.
  Udgivet: (2006-01-01)
• Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses.
  af: Dobson-Stone, C, et al.
  Udgivet: (2000)