香料 发表于 2025-3-26 22:01:28
http://reply.papertrans.cn/43/4273/427208/427208_31.pngSOW 发表于 2025-3-27 01:32:27
http://reply.papertrans.cn/43/4273/427208/427208_32.pngdissent 发表于 2025-3-27 05:49:46
http://reply.papertrans.cn/43/4273/427208/427208_33.png啤酒 发表于 2025-3-27 13:02:46
,Genetics of Hirschsprung’s Disease,s attributed to a disorder of the enteric nervous system (ENS) whereby ganglion cells fail to innervate the lower gastrointestinal tract during embryonic development. HSCR is a complex disease that mainly results from the interaction of several genes and manifests with low, sex-dependent penetranceentitle 发表于 2025-3-27 16:01:20
http://reply.papertrans.cn/43/4273/427208/427208_35.png分散 发表于 2025-3-27 20:06:18
http://reply.papertrans.cn/43/4273/427208/427208_36.pngAccede 发表于 2025-3-28 00:37:29
,Epidemiology and Clinical Characteristics of Hirschsprung’s Disease,ls in the distal bowel beginning at the internal sphincter and extending proximally for varying distances. In the human fetus, neural crest-derived neuroblasts first appear in the developing esophagus at 5 weeks of gestation and then migrate down to the anal canal in a craniocaudal direction duringPALSY 发表于 2025-3-28 05:18:46
,Congenital Anomalies and Genetic Associations in Hirschsprung’s Disease, of normal signalling during development of enteric nerve cells, resulting in aganglionosis of the distal bowel. It is a frequent cause of neonatal intestinal obstruction and beyond..It occurs as an isolated phenotype in 70% but is not infrequently associated with congenital abnormalities (5–32%) anelastic 发表于 2025-3-28 07:18:58
http://reply.papertrans.cn/43/4273/427208/427208_39.pngTOM 发表于 2025-3-28 12:59:06
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