FKBP10 and Bruck Syndrome: Phenotypic Heterogeneity or Call for Reclassification?

Lignende værker

• FKBP10 and Bruck Syndrome: Phenotypic Heterogeneity or Call for Reclassification?
  af: Shaheen, Ranad, et al.
  Udgivet: (2010)
• Mutations in FKBP10 Cause Recessive Osteogenesis Imperfecta and Bruck Syndrome
  af: Kelley, Brian P, et al.
  Udgivet: (2011)
• A null mutation in CABP4 causes Leber’s congenital amaurosis-like phenotype
  af: Aldahmesh, Mohammed A., et al.
  Udgivet: (2010)
• Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients
  af: Zhou, Peiran, et al.
  Udgivet: (2014)
• Mutations in TMEM231 cause Meckel–Gruber syndrome
  af: Shaheen, Ranad, et al.
  Udgivet: (2013)