A boy with dysmorphic features, intellectual disability, and biallelic homozygous deletion in NRXN1

被引：4
|
作者：
Holmquist, Peter [1 ]
机构：
[1] Skane Univ Hosp, Dept Paediat, S-22185 Lund, Sweden
来源：
CLINICAL DYSMORPHOLOGY | 2015年 / 24卷 / 02期
关键词：
D O I：
10.1097/MCD.0000000000000070
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
[No abstract available]
引用
收藏
页码：75 / 78
页数：4
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