Exome sequencing study of non-syndromic hereditary hearing loss. Homo sapiens
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA269160
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资源简介：
Use of exome sequencing and high-resolution array comparative genome hybridization in families and in isolated probands for discovering novel genetic contributors to non-syndromic hereditary hearing loss.
创建时间：
2014-12-03
