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	Detection of ten novel FBN1 mutations in Chinese patients with typical or incomplete Marfan syndrome and an overview of the genotype-phenotype correlations
	Gao, Linggen; Tian, Tao; Zhou, Xianliang; Fan, Li; Wang, Rong; Wu, Haiying
	2019
卷号	293页码:186-191
关键词	Marfan syndrome Aortic aneurysm/dissection FBN1 Mutation Genotype Phenotype
ISSN号	0167-5273
DOI	10.1016/j.ijcard.2019.06.066
URL标识	查看原文
收录类别	SCIE ; PUBMED
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/6338527
专题	中国医学科学院 北京协和医学院
推荐引用方式 GB/T 7714	Gao, Linggen,Tian, Tao,Zhou, Xianliang,et al. Detection of ten novel FBN1 mutations in Chinese patients with typical or incomplete Marfan syndrome and an overview of the genotype-phenotype correlations[J],2019,293:186-191.
APA	Gao, Linggen,Tian, Tao,Zhou, Xianliang,Fan, Li,Wang, Rong,&Wu, Haiying.(2019).Detection of ten novel FBN1 mutations in Chinese patients with typical or incomplete Marfan syndrome and an overview of the genotype-phenotype correlations.,293,186-191.
MLA	Gao, Linggen,et al."Detection of ten novel FBN1 mutations in Chinese patients with typical or incomplete Marfan syndrome and an overview of the genotype-phenotype correlations".293(2019):186-191.

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