Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy

Παρόμοια τεκμήρια

• Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy
  ανά: Poulter, James A., κ.ά.
  Έκδοση: (2010)
• Autosomal dominant exudative vitreoretinopathy.
  ανά: Ober, R R, κ.ά.
  Έκδοση: (1980)
• Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree
  ανά: Toomes, C, κ.ά.
  Έκδοση: (2005)
• Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree
  ανά: Toomes, C, κ.ά.
  Έκδοση: (2005)
• A New Locus for Autosomal Dominant Familial Exudative Vitreoretinopathy Maps to Chromosome 11p12-13
  ανά: Downey, L. M., κ.ά.
  Έκδοση: (2001)