Edinburgh Research Explorer

Whole exome sequencing is a sensitive cost-effective method of detecting mutations in osteogenesis imperfecta and Marfan syndrome.

Research output: Contribution to journalArticle

  • A M MCinerney-Leo
  • M S Marshall
  • B Gardiner
  • P J Coucke
  • L Van Laer
  • B L Loeys
  • Kim Summers
  • S Symoens
  • J A West
  • M J West
  • B P Wordsworth
  • A Zankl
  • P J Leo
  • M A Brown
  • E L Duncan

Related Edinburgh Organisations

Original languageEnglish
Article number456
Number of pages9
JournalBoneKEy reports
Early online date4 Dec 2013
Publication statusPublished - 4 Dec 2013

ID: 12434104