Short-rib polydactyly syndrome presenting with recurrent severe first-trimester phenotypes: the utility of exome sequencing in deciphering variants of DYNC2H1 gene

被引：5
|
作者：
He, Yi [1 ]
Li, Yu-Juan [1 ]
Xu, Li-Li [2 ]
Li, Dong-Zhi [2 ]
机构：
[1] Dongguan Maternal & Children Healthcare Hosp, Prenatal Diag Ctr, Dongguan, Peoples R China
[2] Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R China
来源：
JOURNAL OF OBSTETRICS AND GYNAECOLOGY | 2020年 / 40卷 / 06期
关键词：
PRENATAL-DIAGNOSIS;
D O I：
10.1080/01443615.2019.1655722
中图分类号：
R71 [妇产科学];
学科分类号：
100211 ;
摘要：
[No abstract available]
引用
收藏
页码：874 / 876
页数：3
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