Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

Παρόμοια τεκμήρια

• MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta
  ανά: Kim, J, κ.ά.
  Έκδοση: (2005)
• Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta
  ανά: El-Sayed, Walid, κ.ά.
  Έκδοση: (2009)
• Mutations in RELT cause autosomal recessive amelogenesis imperfecta
  ανά: Kim, Jung‐Wook, κ.ά.
  Έκδοση: (2018)
• Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
  ανά: Hart, T, κ.ά.
  Έκδοση: (2003)
• An autosomal recessive cone–rod dystrophy associated with amelogenesis imperfecta
  ανά: Michaelides, M, κ.ά.
  Έκδοση: (2004)