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	A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis
	Liangjun Yin; Xiaolan Du; Cuiling Li; Xiaoling Xu; Zhi Chen; Nan Su; Ling Zhao; Huabing Qi; Fubing Li; Jing Xue
刊名	Bone
	2008
卷号	Vol.42 No.4页码:631-643
关键词	Fibroblast growth factor receptor 2 Apert syndrome Chondrocyte Osteoblast Mouse model
URL标识	查看原文
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/1841491
专题	四川大学
作者单位	1.Sichuan Univ, W China Ctr Med Sci, Chengdu 610041, Peoples R China Organization-Enhanced Name Sichuan University 2.USA Organization-Enhanced Name NIH National Institute of Diabetes & Digestive & Kidney Diseases National Institutes of Health - USA 3.Chongqing Med Univ, Affiliated Hosp 2, Chongqing 400010, Peoples R China Organization-Enhanced Name Chongqing Medical University 4.NIDDK, NIH, Genet Dev & Dis Branch, Bethesda, MD 5.Third Mil Med Univ, Daping Hosp, Inst Surg Res,Ctr Trauma, State Key Lab Trauma Burns & Combined Injury, Chongqing 400042, Peoples R China Organization-Enhanced Name Third Military Medical University
推荐引用方式 GB/T 7714	Liangjun Yin,Xiaolan Du,Cuiling Li,et al. A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis[J]. Bone,2008,Vol.42 No.4:631-643.
APA	Liangjun Yin.,Xiaolan Du.,Cuiling Li.,Xiaoling Xu.,Zhi Chen.,...&Lin Chen.(2008).A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis.Bone,Vol.42 No.4,631-643.
MLA	Liangjun Yin,et al."A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis".Bone Vol.42 No.4(2008):631-643.

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