相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome
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Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome
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