结论唐氏综合征动物模型16三体鼠伴有先天性巨结肠，这种动物模型可用于研究先天性巨结肠病。
Conclusion trisomy 16 mice occur with congenital megacolon, and trisomy 16 mice may be also regard as an animal model for Hirschsprung's disease.
本研究应用电镜免疫细胞化学方法，对小儿先天性巨结肠病结肠壁内含P物质（SP）神经进行了观察。
The ultrastructure of substance P (SP) neuron in the colon of patients with Hirschsprung's disease was investigated by using immunoelectron microscopic method.
本研究应用电镜免疫细胞化学方法，对小儿先天性巨结肠病结肠壁内含P物质（SP）神经进行了观察。
The ultrastructure of substance P (SP) neuron in the colon of patients with Hirschsprung's disease was investigated by using immunoelectron microscopic method.
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