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. 2018 Oct 5;145(19):dev170019. doi: 10.1242/dev.170019

Fig. 1.

Fig. 1.

The 1D mutation causes exencephaly and spinal cord defects. (A,B) Lateral (left) and dorsal (right) views of E9.5 wild-type and 1D mutant embryos obtained from micro computed tomography (microCT) scans. Arrowheads in B demarcate the extent of exencephaly in the 1D mutant. Lines indicate the level of cross-sections shown in C-F. (C-F) Cross sections through the hindbrain (C,D) and spinal cord (E,F) regions in E9.5 wild type and 1D mutants. Black arrowheads point to the medial hinge point. Unfilled arrowhead in F points to the surface epithelia covering the abnormally shaped neuroepithelia in 1D embryos. Scale bars: 300 µm (A,B); 100 µm (C-F).