A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome

出版年份 2011 全文链接

标题

作者

关键词

出版物

Volume 12, Issue 1, Pages -

出版商

Springer Nature

发表日期

2011-09-24

DOI

10.1186/1471-2350-12-122

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