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	Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population
	Lu, Nanhang; Wang, Jinzeng; Zhu, Bijun; Zhang, Miaomiao; Qi, Fazhi; Wang, Xiangdong; Gu, Jianying
刊名	CANCER BIOMARKERS
	2018
卷号	21期号:1
关键词	Gorlin syndrome nevoid basal cell carcinoma syndrome whole exome sequencing Single-nucleotide variants ZFHX4
ISSN号	1574-0153
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/3609024
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Lu, Nanhang,Wang, Jinzeng,Zhu, Bijun,et al. Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population[J]. CANCER BIOMARKERS,2018,21(1).
APA	Lu, Nanhang.,Wang, Jinzeng.,Zhu, Bijun.,Zhang, Miaomiao.,Qi, Fazhi.,...&Gu, Jianying.(2018).Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population.CANCER BIOMARKERS,21(1).
MLA	Lu, Nanhang,et al."Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population".CANCER BIOMARKERS 21.1(2018).

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