Whole genome sequencing implicates rare variants in sporadic Hirschsprung disease

被引：0
|
作者：
Tang, C. S. [1 ]
Cherny, S. S. [1 ]
Sham, P. C. [1 ]
Tam, P. P. K. H. [1 ]
Garcia-Barcelo, M. M. [1 ]
机构：
[1] Univ Hong Kong, Hong Kong, Peoples R China
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：
P03.20D
引用
收藏
页码：206 / 206
页数：1
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