A prospective evaluation of exome sequencing in 51 fetuses with multiple congenital anomalies and lessons for future prenatal implementation

被引：0

作者：

Yeung, A. ^{[1
,2
,3
]}

Chan, F. ^{[3
,4
]}

Vasudevan, A. ^{[5
]}

Collett, J. ^{[3
,4
]}

Prystupa, S. ^{[6
]}

Chan, Y. ^{[6
]}

McGillivray, G. ^{[1
,3
,5
]}

机构：

[1] Murdoch Childrens Res Inst, Victorian Clin Genet Serv, Parkville, Vic, Australia

[2] Monash Hlth, Monash Genet, Melbourne, Australia

[3] Melbourne Genom Hlth Alliance, Melbourne, Vic, Australia

[4] Royal Womens Hosp, Dept Anat Pathol, Parkville, Vic, Australia

[5] Royal Womens Hosp, Dept Clin Genet, Parkville, Vic, Australia

[6] Monash Hlth, Dept Anat Pathol, Melbourne, Vic, Australia

来源：

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：

P01.22B

引用

页码：1183 / 1184

页数：2