The transition of fetal haematopoietic sites in mice was examined histologically from 12.5‐day embryos (E12.5) until 10 days of age (D10), and the expression of the adhesive molecules VCAM‐1 and fibronectin was examined immunohistologically. Erythropoiesis occurred in the liver (E12.5–18.5), spleen (E18.5–D4) and bone marrow (D6–10), in that sequence. Even at D10, some erythropoiesis occurred in the liver, and more so in the spleen, although the active haematopoietic site was the bone marrow. Similarly, granulopoiesis of neutrophils occurred in the liver, spleen and bone marrow in turn. Granulopoiesis still occurred in the spleen at D10, but no neutrophils were found in the liver after D4. VCAM‐1 appeared in the liver, spleen and bone marrow in parallel with active erythropoiesis and granulopoiesis. The co‐expression of VCAM‐1 and fibronectin was recognized in the endothelial cells of the sinus at the onset of haematopoiesis. This study showed that haematopoiesis in the liver, spleen and bone marrow overlapped peri‐natally, although it shifted sequentially. VCAM‐1 appears to be closely associated with erythropoiesis and granulopoiesis, and the co‐expression of VCAM‐1 and fibronectin plays a role in inducing haematopoietic stem cells to move to the tissues.