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	Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations
	Villanueva, Carine; Jacobson-Dickman, Elka; Xu, Cheng; Manouvrier, Sylvie; Dwyer, Andrew A.; Sykiotis, Gerasimos P.; Beenken, Andrew; Liu, Yang; Tommiska, Johanna; Hu, Youli
刊名	GENETICS IN MEDICINE
	2015
卷号	17期号:8
关键词	congenital hypogonadotropic hypogonadism fibroblast growth factor receptor 1 FGF receptor substrate 2 alpha split hand/foot malformation
ISSN号	1098-3600
URL标识	查看原文
语种	英语
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4872887
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Villanueva, Carine,Jacobson-Dickman, Elka,Xu, Cheng,et al. Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations[J]. GENETICS IN MEDICINE,2015,17(8).
APA	Villanueva, Carine.,Jacobson-Dickman, Elka.,Xu, Cheng.,Manouvrier, Sylvie.,Dwyer, Andrew A..,...&Pitteloud, Nelly.(2015).Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations.GENETICS IN MEDICINE,17(8).
MLA	Villanueva, Carine,et al."Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations".GENETICS IN MEDICINE 17.8(2015).

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