Fig. 2. Phenotype of the C4st1gt mutation at E19.5 of
embryogenesis. (A) Gross morphology of wild-type (part i, +/+) and
C4st1gt/gt embryos (ii, part gt/gt). (B-H) Alcian
blue/Alizarin Red skeletal stains. (B) Multiple skeletal abnormalities are
evident in mutant embryos. (C) Higher magnification of hind limbs, showing the
severely shortened and thickened iliac bone (i), femur (f) and tibia and
fibula (ti). Arrowhead indicates Alcian Blue staining of cartilage. (D)
Vertebrae in the mutant display misshapen dorsal arches (arrowhead). (E)
Reduced size of scapula (double-headed while arrow) in mutant embryos. (F)
Phalanges 2 and 3, and the talus bone (arrow) fail to ossify in mutant
hindlimbs (m, metatarsal bones). (G) Lateral view and (H) dorsal view of
skull, showing normal size of frontal (a), parietal (b), interparietal (c) and
supraoccipital (d) bones in mutant embryos, but smaller maxilla (arrowhead),
mandible (arrow) and nasal bones in mutant embryos.