SciHub
文献互助
期刊查询
一搜即达
科研导航
即时热点
交流社区
登录
注册
发布
文献
求助
首页
我的求助
捐赠本站
喝一碗糖粥
Lv1
8 积分
2023-12-07 加入
最近求助
最近应助
互助留言
Clinical features and genotype–phenotype correlations in epilepsy patients with de novo DYNC1H1 variants
2小时前
待确认
Clinical Actionability of Genetic Findings in Cerebral Palsy
3天前
已完结
Clinical Actionability of Genetic Findings in Cerebral Palsy
3天前
已完结
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy
4个月前
已完结
Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy
5个月前
已完结
Causal association between epilepsy and its DNA methylation profile and atrial fibrillation
5个月前
已关闭
Causal association between epilepsy and its DNA methylation profile and atrial fibrillation
5个月前
已完结
The role of copy number variants in the genetic architecture of common familial epilepsies
6个月前
已完结
Female Sex Steroids and Epilepsy Part 2: A Practical and Human Focus on Catamenial Epilepsy
6个月前
已完结
Genotype–phenotype associations in 1018 individuals with SCN1A‐related epilepsies
6个月前
已完结
没有进行任何应助
不要水印
5个月前
自己下载了【积分已退回】
6个月前
第二次求助这篇文献了,两次都无法打开,提示文件有损坏
8个月前
我打不开文件
8个月前
最近帖子
最近评论
没有发布任何帖子
没有发布任何评论