Added value of clinical whole-genome sequencing: Cooccurring rare diseases and pharmacogenetic profiling

被引：0
|
作者：
Caspar, S. M. [1 ,2 ]
Najafi, A. [1 ]
Meienberg, J. [1 ]
Schneider, T. [1 ]
Henggeler, C. [1 ]
Matyas, G. [1 ]
机构：
[1] Ctr Cardiovasc Genet & Gene Diagnost, Schlieren, Switzerland
[2] Swiss Fed Inst Technol, Lab Translat Nutr Biol, Zurich, Switzerland
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2020年 / 28卷 / SUPPL 1期
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：
P18.66.A
引用
收藏
页码：698 / 698
页数：1
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