医学文献 >>
  • 检索发现
  • 增强检索
知识库 >>
  • 临床诊疗知识库
  • 中医药知识库
评价分析 >>
  • 机构
  • 作者
默认
×
热搜词:
换一批
论文 期刊
取消
高级检索

检索历史 清除

Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy

广告
第一作者: Arndt,A.-K.
作者单位: Max-Delbruck-Center for Molecular Medicine (MDC), 13125 Berlin, Germany, Department of [1] National Heart and Lung Institute, Imperial College, London SW7 2AZ, United Kingdom, NIHR Royal [2] Institute of Medical Genetics and Human Genetics, Charité University Medicine Berlin, 13353 Berlin [3] Max-Delbruck-Center for Molecular Medicine (MDC), 13125 Berlin, Germany [4] Department of Pathology, German Heart Institute Berlin, 13353 Berlin, Germany [5] Experimental and Clinical Research Center (ECRC), Charité Medical Faculty and Max-Delbruck-Center [6] Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, and Harvard Stem [7] Department of Congenital Heart Defects and Pediatric Cardiology, German Heart Institute Berlin [8] Max-Delbruck-Center for Molecular Medicine (MDC), 13125 Berlin, Germany, DZHK (German Centre for [9] Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115 [10] Department of Congenital Heart Disease and Pediatric Cardiology, University Hospital of Schleswig [11] Institute of Human Genetics, Christian-Albrechts-University Kiel and University Hospital Schleswig [12] National Heart and Lung Institute, Imperial College, London SW7 2AZ, United Kingdom, National Heart [13] Cardiovascular Center, University Hospital Zürich, 8001 Zürich, Switzerland [14]
发布时间 2013-11-20
提交
  • 浏览2
The American Journal of Human Genetics

相似文献

  • 中文期刊
  • 外文期刊
  • 学位论文
  • 会议论文

加载中!

加载中!

加载中!

加载中!

法律状态公告日 法律状态 法律状态信息

特别提示:本网站仅提供医学学术资源服务,不销售任何药品和器械,有关药品和器械的销售信息,请查阅其他网站。

  • 客服热线:4000-115-888 转3 (周一至周五:8:00至17:00)

  • |
  • 客服邮箱:yiyao@wanfangdata.com.cn

  • 违法和不良信息举报电话:4000-115-888,举报邮箱:problem@wanfangdata.com.cn,举报专区

官方微信
万方医学小程序
new医文AI 翻译 充值 订阅 收藏 移动端

官方微信

万方医学小程序

使用
帮助
Alternate Text
调查问卷