6 Clinical genetics of syn- and brachydactyly: mutations in FGFR2 and HOXD13

Lignende værker

• Missense Mutations in the Homeodomain of HOXD13 Are Associated with Brachydactyly Types D and E
  af: Johnson, David, et al.
  Udgivet: (2003)
• P9 Functions of ALX4 and MSX2 in ossification of the skull vault
  af: Antonopoulou, I, et al.
  Udgivet: (2002)
• 18 Muscle and tendon pattern is altered independently of skeletal pattern in HoxD mutant limbs
  af: Ashby, P, et al.
  Udgivet: (2002)
• Mutations in HOXD13 Underlie Syndactyly Type V and a Novel Brachydactyly-Syndactyly Syndrome
  af: Zhao, Xiuli , et al.
  Udgivet: (2007)
• 4 Fgfr2/b is required for the morphogenic migration of the limb bud ectoderm
  af: Gorivodsky, M, et al.
  Udgivet: (2002)