Detecting copy number variations in routine diagnostic samples using next generation sequencing data

被引：0
|
作者：
Singh, Ashish Kumar [1 ]
Johansen, Jostein [2 ]
Ravi, Anuradha [2 ]
Misund, Kristine [2 ]
机构：
[1] St Olavs Hosp, Dept Med Genet, Trondheim, Norway
[2] St Olavs Hosp, Dept Med Genet, Trondheim, Norway
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P17.023.C
引用
收藏
页码：639 / 639
页数：1
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