Prenatal exome sequencing analysis in the clinical setting of fetuses with structural anomalies or increased nuchal translucency

被引：0
|
作者：
Lazar, Roni Zemet [1 ]
Meng, Linyan [2 ]
Liu, Pengfei [2 ]
Dai, Hongzheng [2 ]
Xia, Fan [2 ]
Eng, Christine [2 ]
Van Den Veyver, Ignatia [1 ,3 ]
Vossaert, Liesbeth [2 ]
机构：
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Genet, Houston, TX USA
[3] Baylor Coll Med, Dept Obstet & Gynecol, Houston, TX 77030 USA
来源：
GENETICS IN MEDICINE | 2022年 / 24卷 / 03期
关键词：
D O I：
10.1016/j.gim.2022.01.507
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
eP474
引用
收藏
页码：S301 / S301
页数：1
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