Structural and segregation analysis of the type II collagen gene (COL2A1) in some heritable chondrodysplasias.

Gelijkaardige items

• SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia.
  door: Sweetman, W A, et al.
  Gepubliceerd in: (1992)
• Evidence against the structural gene encoding type II collagen (COL2A1) as the mutant locus in achondroplasia.
  door: Ogilvie, D, et al.
  Gepubliceerd in: (1986)
• Exclusion of the alpha 1(II) collagen structural gene as the mutant locus in type II Ehlers-Danlos syndrome.
  door: Wordsworth, P, et al.
  Gepubliceerd in: (1985)
• Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasia.
  door: Wallis, G A, et al.
  Gepubliceerd in: (1996)
• Segregation of all four major fibrillar collagen genes in the Marfan syndrome.
  door: Ogilvie, D J, et al.
  Gepubliceerd in: (1987)