Whole-genome sequencing for prenatal diagnosis of congenital malformations: a prospective cohort study in a clinical setting

被引：0
|
作者：
Conner, P. [3 ]
Westenius, E. [1 ]
Sahlin, E. [1 ]
Papadogiannakis, N. [2 ]
Lindstrand, A. [1 ]
Iwarsson, E. [1 ]
机构：
[1] Karolinska Univ Hosp, Karolinska Inst, Dept Mol Med & Surg, Clin Genet, Stockholm, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Dept Lab Med, Pathol, Huddinge, Sweden
[3] Karolinska Univ Hosp, Karolinska Inst, Dept Womens & Childrens Hlth, Ctr Fetal Med, Stockholm, Sweden
来源：
ULTRASOUND IN OBSTETRICS & GYNECOLOGY | 2023年 / 62卷
关键词：
D O I：
10.1002/uog.26787
中图分类号：
O42 [声学];
学科分类号：
070206 ; 082403 ;
摘要：
EP11.03
引用
收藏
页码：160 / 160
页数：1
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