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	C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients
	Lin, Ying[1]; Gao, Hongbin[2,3]; Ai, Siming[1]; Eswarakumar, Jacob V. P.[4]; Chen, Chuan[1,5]; Zhu, Yi[1,5]; Li, Tao[1]; Liu, Bingqian[1]; Liu, Xialin[1]; Luo, Lixia[1]
刊名	MOLECULAR MEDICINE REPORTS
	2017
卷号	16页码:5333-5337
关键词	craniosynostosis fibroblast growth factor receptor 2 gene mutation Peters anomaly Pfeiffer syndrome Crouzon syndrome
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/2186803
专题	华南理工大学
作者单位	1.[1]Sun Yat Sen Univ, Zhongshan Ophthalm Ctr, State Key Lab Ophthalmol, 54 Xianlie South Rd, Guangzhou 510060, Guangdong, Peoples R China 2.[2]Guangdong Lab Anim Monitoring Inst, Key Prov Lab Guangdong Lab Anim, Guangzhou 510663, Guangdong, Peoples R China 3.[3]Southern Med Univ, Sch Publ Hlth & Trop Med, Dept Toxicol, Guangzhou 510515, Guangdong, Peoples R China 4.[4]Yale Univ, Sch Med, Dept Pharmacol, 333 Cedar St, New Haven, CT 06520 USA 5.[5]Univ Miami, Miller Sch Med, Dept Mol & Cellular Pharmacol, Miami, FL 33136 USA 6.[6]Sun Yat Sen Univ, Affiliated Hosp 1, Dept Obstet & Gynecol, Guangzhou 510000, Guangdong, Peoples R China
推荐引用方式 GB/T 7714	Lin, Ying[1],Gao, Hongbin[2,3],Ai, Siming[1],et al. C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients[J]. MOLECULAR MEDICINE REPORTS,2017,16:5333-5337.
APA	Lin, Ying[1].,Gao, Hongbin[2,3].,Ai, Siming[1].,Eswarakumar, Jacob V. P.[4].,Chen, Chuan[1,5].,...&Lu, Lin[1].(2017).C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients.MOLECULAR MEDICINE REPORTS,16,5333-5337.
MLA	Lin, Ying[1],et al."C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients".MOLECULAR MEDICINE REPORTS 16(2017):5333-5337.

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