Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype

出版年份 2016 全文链接

标题

作者

关键词

出版物

Volume 11, Issue 6, Pages 2247-2253

出版商

Spandidos Publications

发表日期

2016-04-11

DOI

10.3892/etm.2016.3241

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