Fragilitas ossium: a new autosomal recessive mutation in the mouse

J Hered. 1981 Nov-Dec;72(6):440-1. doi: 10.1093/oxfordjournals.jhered.a109554.

Abstract

Fragilitas ossium, fro, is an often lethal recessive mutation that was discovered in a randombred stock of mice after treatment with the chemical mutagen tris(1-aziridinyl) phosphine-sulphine. The fro/fro mice have osteoporosis-bending and fracture of the long bones-that is associated with apparently normal cartilage growth. The roentgenological and pathological features are similar to those of the severe, often lethal recessive form of human osteogenesis imperfecta.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal*
  • Female
  • Genes, Recessive
  • Male
  • Mice
  • Mice, Mutant Strains / genetics*
  • Mutation*
  • Osteogenesis Imperfecta*
  • Osteoporosis / genetics
  • Osteoporosis / veterinary*
  • Rodent Diseases / genetics
  • Thiotepa

Substances

  • Thiotepa