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The SEMA3A rs7804122 polymorphism is associated with Hirschsprung disease in the northeastern region
期刊名称:Birth Defects Res A Clin Mol Teratol
时间:2012.2.1
页码:91-95
相关项目:FHL1基因在先天性马蹄内翻足肌肉表型形成中的作用机制研究
作者:
Wang LL|Fan Y|Zhou FH|Li H|Zhang Y|Miao JN|Gu H|Huang TC|Yuan ZW|
同期刊论文项目
FHL1基因在先天性马蹄内翻足肌肉表型形成中的作用机制研究
期刊论文 10
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HOXD13 may play a role in idiopathic congenital clubfoot by regulating the expression of FHL1
Transcriptional regulation of Fhl1 by estradiol in rat myoblastocytes
Up-regulated FHL1 Expression Maybe Involved in the Prognosis of Hirschsprung's Disease
Mutations and Down-Regulation of CDX1 in Children with Anorectal Malformations
miR-9*- and miR-124a-Mediated Switching of Chromatin Remodelling Complexes is Altered in Rat Spina B
FHL1在骨骼肌发育中的作用及其与人类肌病的关系