Pittsburgh Heterotaxy Study
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下载链接：
https://www.ncbi.nlm.nih.gov/sra/SRP171605
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资源简介：
To understand the genetic etiology of heterotaxy, patients with heterotaxy were consented and recruited, with blood drawn for DNA extraction and exome sequencing. Using the exome sequencing dataset obtained, rare coding sequence variants were identified.
创建时间：
2019-11-06
