A rare mosaic 22q11.2 microdeletion identified in a Chinese family with recurrent fetal conotruncal defects | |
Sheng, Wei; Li, Xiaodi; Sun, Liqun; Huang, Guoying; Chen, Weicheng | |
刊名 | MOLECULAR GENETICS & GENOMIC MEDICINE |
2019 | |
卷号 | 7期号:8 |
关键词 | 22q11 2 microdeletion syndrome chromosomal microarray analysis fluorescence in situ hybridisation mosaic fetal conotruncal defects |
ISSN号 | 2324-9269 |
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/3595042 |
专题 | 复旦大学上海医学院 |
推荐引用方式 GB/T 7714 | Sheng, Wei,Li, Xiaodi,Sun, Liqun,et al. A rare mosaic 22q11.2 microdeletion identified in a Chinese family with recurrent fetal conotruncal defects[J]. MOLECULAR GENETICS & GENOMIC MEDICINE,2019,7(8). |
APA | Sheng, Wei,Li, Xiaodi,Sun, Liqun,Huang, Guoying,&Chen, Weicheng.(2019).A rare mosaic 22q11.2 microdeletion identified in a Chinese family with recurrent fetal conotruncal defects.MOLECULAR GENETICS & GENOMIC MEDICINE,7(8). |
MLA | Sheng, Wei,et al."A rare mosaic 22q11.2 microdeletion identified in a Chinese family with recurrent fetal conotruncal defects".MOLECULAR GENETICS & GENOMIC MEDICINE 7.8(2019). |
个性服务 |
查看访问统计 |
相关权益政策 |
暂无数据 |
收藏/分享 |
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。
修改评论