Alanna E. KoehlerNational Institutes of Health Undiagnosed Diseases Program NIH关注立即认领分享关注立即认领分享基本信息浏览量:0职业迁徙个人简介暂无内容研究兴趣论文共 2 篇作者统计合作学者相似作者按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选时间引用量主题期刊级别合作者合作机构Kilquist Syndrome: A Novel Syndromic Hearing Loss Disorder Caused by Homozygous Deletion of SLC12A2Ellen F Macnamara,Alanna E Koehler,Precilla D'Souza,Tyra Estwick,Paul Lee,Gilbert Vezina, , Harper Fauni,Stephen R Braddock,Erin Torti,James Matthew Holt,Prashant Sharma,HUMAN MUTATION(2019)引用37浏览0WOS引用370Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion ofSLC12A2Ellen Macnamara,Alanna E. Koehler, Precilla D’Souza,Tyra Estwick,Paul Lee,Gilbert Vézina, Harper B Fauni,Stephen R. Braddock,Erin Torti,James Holt,Prashant Sharma,May Christine V. Malicdan,Human Mutationno. 5 (2019): 532-538引用10浏览0引用100作者统计合作学者合作机构D-Core合作者学生导师暂无相似学者,你可以通过学者研究领域进行搜索筛选数据免责声明页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果,我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问,可以通过电子邮件方式联系我们:report@aminer.cn