Detecting disease-causing genetic variants in 48 patients with familial colorectal cancer by using whole exome sequencing

被引：0
|
作者：
Singh, Ashish Kumar [1 ,2 ]
Talseth-Palmer, Bente [3 ,4 ,5 ]
Xavier, Alexandre [3 ,4 ]
Scott, Rodney J. [3 ,4 ,6 ]
Drablos, Finn [2 ]
Sjursen, Wenche [1 ,2 ]
机构：
[1] St Olavs Hosp, Dept Med Genet, Trondheim, Norway
[2] NTNU Norwegian Univ Sci & Technol, Dept Clin & Mol Med, Fac Med & Hlth Sci, Trondheim, Norway
[3] Univ Newcastle, Newcastle, NSW, Australia
[4] Hunter Med Res Inst, Sch Biomed Sci & Pharm, Fac Hlth & Med, Newcastle, NSW, Australia
[5] More & Romsdal Hosp Trust, Res Unit, Alesund, Norway
[6] NSW Hlth Pathol, Newcastle, NSW, Australia
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31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：
EP13.007
引用
收藏
页码：247 / 247
页数：1
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