Additional file 1: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
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资源简介:
List of phenotypes potentially related to hearing defects used as keywords for initial query on HGMD. (XLSX 16 kb)
本数据集为与听力缺陷潜在相关的表型列表,用作人类基因突变数据库(Human Gene Mutation Database, HGMD)初始检索的关键词,文件格式为XLSX,大小16 KB。
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figshare创建时间:
2018-11-08



