USING PHARMACOGENOMICS IN CLINICAL TREATMENT OF CHILDREN WITH FRAGILE X SYNDROME AND SEX CHROMOSOME ANEUPLOIDY

被引：0
|
作者：
Tartaglia, N. R. [1 ,2 ]
Howell, S. E. [1 ,2 ]
机构：
[1] Univ Colorado, Sch Med, Aurora, CO USA
[2] Childrens Hosp Colorado, Dev Pediat, Aurora, CO USA
来源：
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH | 2017年 / 61卷 / 09期
关键词：
fragile X; pharmacogenomic testing; sex chromosomes; XXY;
D O I：
暂无
中图分类号：
G76 [特殊教育];
学科分类号：
040109 ;
摘要：
引用
收藏
页码：831 / 832
页数：2
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