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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).
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