机构：[1]Capital Med Univ, Beijing Childrens Hosp, Beijing, Peoples R China;首都医科大学附属北京儿童医院[2]Beijing Pediat Res Inst, Beijing Key Lab Genet Birth Defects, Beijing, Peoples R China;[3]Natl Ctr Childrens Hlth, Genet & Birth Defects Control Ctr, Beijing, Peoples R China;[4]MOE Key Lab Major Dis Children, Beijing, Peoples R China
出处：
ISSN：
基金：
Ministry of Science and Technology of ChinaMinistry of Science and Technology, China [2016YFC1000306]; Beijing Municipal Commission of Health and Family Planning Foundation [PXM2017_026274_000001]
第一作者机构：[1]Capital Med Univ, Beijing Childrens Hosp, Beijing, Peoples R China;[2]Beijing Pediat Res Inst, Beijing Key Lab Genet Birth Defects, Beijing, Peoples R China;[3]Natl Ctr Childrens Hlth, Genet & Birth Defects Control Ctr, Beijing, Peoples R China;[4]MOE Key Lab Major Dis Children, Beijing, Peoples R China
推荐引用方式(GB/T 7714)：
Guo R.,Hao C.,Qian S.,et al.Novel ABCC9 missense mutation in a Chinese infant with Cantu syndrome without skeletal manifestations[J].EUROPEAN JOURNAL OF HUMAN GENETICS.2019,27:1306-1307.
APA：
Guo, R.,Hao, C.,Qian, S.&Li, W..(2019).Novel ABCC9 missense mutation in a Chinese infant with Cantu syndrome without skeletal manifestations.EUROPEAN JOURNAL OF HUMAN GENETICS,27,
MLA：
Guo, R.,et al."Novel ABCC9 missense mutation in a Chinese infant with Cantu syndrome without skeletal manifestations".EUROPEAN JOURNAL OF HUMAN GENETICS 27.(2019):1306-1307
