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Fig. 4. C3Ggt/gt mutant phenotype. Homozygous mutant embryos at
E11.5 (A-C), E13.5 (D,E), E14.5 (F, dead), and (G-I) Haematoxylin and
Eosinstained paraffin sections at E11.5. Note the formation of haemorrhages in
the majority of cases (E10.5-E11.5), which initiated near the hindbrain
neuroepithelium (arrows in A,B,G). These haemorrhages enlarged (H) and finally
the neuroepithelium ruptured (arrow in I). In other cases, embryos exhibited
massive subcutaneous oedema and haemorrhagic oedema at E13.5 (arrows in D,E).
Bar represents 77 µm in A-C, 150 µm in D,E, 190 µm in F, 106 µm in
G, 66 µm in H and 80 µm in I.