Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
作者:
发布时间
2013-11-20
- 浏览0
Journal of Medical Genetics
195-203页
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文


换一批



