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

Παρόμοια τεκμήρια

• FKBP10 and Bruck Syndrome: Phenotypic Heterogeneity or Call for Reclassification?
  ανά: Shaheen, Ranad, κ.ά.
  Έκδοση: (2010)
• Mutations in FKBP10 Cause Recessive Osteogenesis Imperfecta and Bruck Syndrome
  ανά: Kelley, Brian P, κ.ά.
  Έκδοση: (2011)
• A null mutation in CABP4 causes Leber’s congenital amaurosis-like phenotype
  ανά: Aldahmesh, Mohammed A., κ.ά.
  Έκδοση: (2010)
• Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients
  ανά: Zhou, Peiran, κ.ά.
  Έκδοση: (2014)
• Natural human knockouts and the era of genotype to phenotype
  ανά: Alkuraya, Fowzan S
  Έκδοση: (2015)