Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy

Схожие документы

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