Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome

出版年份 2010 全文链接

标题

作者

关键词

出版物

Volume 18, Issue 11, Pages 1196-1201

出版商

Springer Nature

发表日期

2010-06-30

DOI

10.1038/ejhg.2010.102

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