Phenotype-Genotype Correlations in Mouse Models of Amelogenesis Imperfecta Caused by Amelx and Enam Mutations

समान संसाधन

• Amelogenesis Imperfecta Due to a Mutation of the Enamelin Gene: Clinical Case With Genotype-phenotype Correlations
  द्वारा: Lindemeyer, Rochelle G., और अन्य
  प्रकाशित: (2010)
• Novel ENAM and LAMB3 Mutations in Chinese Families with Hypoplastic Amelogenesis Imperfecta
  द्वारा: Wang, Xin, और अन्य
  प्रकाशित: (2015)
• A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta
  द्वारा: Barron, Martin J., और अन्य
  प्रकाशित: (2010)
• Amelogenesis Imperfecta: Genotype-Phenotype Studies in 71 Families
  द्वारा: Wright, J. Timothy, और अन्य
  प्रकाशित: (2011)
• Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
  द्वारा: Hart, T, और अन्य
  प्रकाशित: (2003)