文
论文分享
演练场
杂货铺
论文推荐
字
编辑器下载
登录
注册
Sporadic NF1 mutation associated with a de-novo 20q11.3 deletion explains the association of unusual facies, Moyamoya vasculopathy, and developmental delay, reported by Bertoli et al. in 2009.
复制论文ID
分享
摘要
作者
参考文献
暂无分享,去
创建一个
N. Boddaert
|
D. Vidaud
|
S. Lyonnet
|
C. Santoro
|
V. Malan
|
M. Bertoli
保存到论文桶