Hirschsprung disease caused by a de novo interstitial deletion of 13q21.33-q31.1

被引：0
|
作者：
Mueller-Hofstede, C. B. [1 ]
Siebers-Renelt, U. [1 ]
Wieacker, P. [1 ]
Roepke, A. [1 ]
机构：
[1] Inst Human Genet & Anthropol, Munster, Germany
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-P11.24
引用
收藏
页码：1877 / 1877
页数：1
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