X-linked syndromic mental retardation, Nascimento - type identified by Whole Exome Sequencing

被引：0
|
作者：
Kenteroglou, O. [1 ]
Tsoutsou, E. [1 ]
Sofocleous, C. [1 ]
Veltra, D. [1 ]
Psoni, S. [1 ]
Amenta, S. [1 ]
Willems, P. [2 ]
Fryssira, H. [1 ]
机构：
[1] Choremio Reasearch Lab, Athens, Greece
[2] GENDIA, Antwerp, Belgium
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27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-P08.32
引用
收藏
页码：953 / 954
页数：2
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