Molecular heterogeneity in the mild autosomal dominant forms of osteogenesis imperfecta.

Benzer Materyaller

• Use of molecular haplotypes specific for the human pro alpha 2(I) collagen gene in linkage analysis of the mild autosomal dominant forms of osteogenesis imperfecta.
  Yazar:: Falk, C T, ve diğerleri
  Baskı/Yayın Bilgisi: (1986)
• Transgenic mouse model of the mild dominant form of osteogenesis imperfecta.
  Yazar:: Bonadio, J, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)
• Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta.
  Yazar:: Tsipouras, P, ve diğerleri
  Baskı/Yayın Bilgisi: (1983)
• Genotype-Phenotype Correlations in Autosomal Dominant Osteogenesis Imperfecta
  Yazar:: I. Mouna Ben Amor, ve diğerleri
  Baskı/Yayın Bilgisi: (2011-01-01)
• Genotype-Phenotype Correlations in Autosomal Dominant Osteogenesis Imperfecta
  Yazar:: Ben Amor, I. Mouna, ve diğerleri
  Baskı/Yayın Bilgisi: (2011)