Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product

被引：0
作者：
Zhang, Honghong
Sun, Yixi
Zhu, Yuxia
Hong, Jiali
Zheng, Miaomiao
机构：
来源：
FRONTIERS IN PEDIATRICS | 2022年 / 10卷
关键词：
Rett syndrome; MECP2; prenatal diagnosis; mosaicism; heteroduplexes;
D O I：
10.3389/fped.2022.823860
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
引用
收藏
页数：2
相关论文
共 1 条
[1]   Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product [J].
Zhang, Honghong ;
Sun, Yixi ;
Zhu, Yuxia ;
Hong, Jiali ;
Zheng, Miaomiao .
FRONTIERS IN PEDIATRICS, 2021, 9
1