Detection of clinically relevant exonic copy number changes in fetuses by chromosomal microarray analysis

被引：0
|
作者：
Owen, Nichole [1 ,2 ]
Okur, Volkan [1 ,2 ]
Anderson, Stephanie [2 ]
Smith, Janice [1 ,2 ]
Bacino, Carlos [1 ,2 ]
Ward, Patricia [1 ,2 ]
Cheung, Sau [1 ]
Breman, Amy [1 ,2 ]
Van Den Veyver, Ignatia [1 ]
Bi, Weimin [1 ,2 ]
机构：
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Genet, Houston, TX USA
来源：
GENETICS IN MEDICINE | 2022年 / 24卷 / 03期
关键词：
D O I：
10.1016/j.gim.2022.01.495
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
eP462
引用
收藏
页码：S291 / S291
页数：1
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