首页> 外文期刊>European journal of human genetics: EJHG >Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population (vol 27, pg 1235, 2019)
【24h】

Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population (vol 27, pg 1235, 2019)

机译:与芬兰人群的CRADD创始人变异相关的表型谱相关(Vol 27,PG 1235,2019)

获取原文
获取原文并翻译 | 示例
           

摘要

An amendment to this paper has been published and can be accessed via a link at the top of the paper.
机译:已发布对本文的修订,并可通过纸张顶部的链接访问。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号