Clinical and genetic analysis of four Czech families with 15q13.3 microdeletion syndrome

被引：0
|
作者：
Cejnova, V. [1 ]
Vancova, L. [1 ]
Liskova, L. [1 ]
Harmas, V. [1 ]
Tothova, M. [2 ]
Fiser, M. [2 ]
Soukupova, M. [1 ]
Lastuvkova, J. [1 ]
机构：
[1] Masaryk Hosp Usti Nad Labem, Reg Hlth Corp, Dept Med Genet, Usti Nad Labem, Czech Republic
[2] GENVIA, Prague, Czech Republic
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2018年 / 26卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
E-P09.01
引用
收藏
页码：936 / 937
页数：2
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