Broadening the phenotype associated with mutations in UPF3B: Two further cases with renal dysplasia and variable developmental delay

出版年份 2012 全文链接

标题

Broadening the phenotype associated with mutations in UPF3B: Two further cases with renal dysplasia and variable developmental delay

作者

关键词

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出版物

European Journal of Medical Genetics

Volume 55, Issue 8-9, Pages 476-479

出版商

Elsevier BV

发表日期

2012-04-26

DOI

10.1016/j.ejmg.2012.03.010

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